clinical research associate training course

Clinical Research Associate

Clinical Research Associate Certification

Clinical research associate certificate will help you get hired or promoted in clinical research monitoring jobs. Gain knowledge to be successful with advanced clinical research associate training. Join one of the best clinical research associate training programs to show your skills as a clinical research monitor.

CRA Training Program

CRAs monitor clinical trial sites for compliance with guidelines and protocols. Salary of $60k to 120k+ based on experience level.

Requirement

A minimum of 4 year degree in science required though scientists, IMGs, nurses, prior coordinators, and even senior CRAs take our course.

Takes 2-4 weeks. Start today. Self-paced. 3k+ enrollees choose us because of our advanced curriculum with practice applications and competitive pricing.

Certification

Triple-accredited course with 17.5 CME. Achieve 70% on 2 attempts on MCQ exam.

Clinical Research Associate Training

Advanced Clinical Research Associate Certification (ACRAC)

Introduction

CME Handout

Common Terminology Used In Clinical Research - Reference Glossary

Commonly Used Abbreviations and Terms in Clinical Research

Roles and Relationships in Clinical Trials

Duties and Responsibilities of a Clinical Research Associate (CRA, Monitor)

Stakeholders in Clinical Trials (Sponsor, Project Manager, IRB, PI, CRA, CRC, Site Staff, Data Team/DSMB, Patients)

Communication between Blinded and Unblinded Staff

Contract Research Organizations (Delegation, Responsibilities, Management )

Sponsor and Investigator Roles

ICH GCP E6 Sections 2-4 Principles, IRB, & Investigator Roles

ICH GCP E6 Section 4 - Reporting Responsibilities of the Investigators

ICH GCP E6 Section 5 - Sponsor/CRO Responsibilities

Clinical Trial Design

Advanced Designs of Clinical Trials

Advanced Review of Phases of Clinical Trials (Preclinical & Phase 0-4)

Randomized Controlled Trials (Randomization, Allocation Concealment, Validity, Blinding, Controls, Outcomes, Fidelity)

Blinding and Unblinding in Clinical Trials

ICH GCP - Overview

An Introduction to Clinical Research

An Overview of ICH GCP

ICH GCP - Ethical Research in Vulnerable Populations

Ethics of Research Involving Children

Ethics of Research Involving Mentally Incapacitated

Ethics of Research Involving Prisoners

Ethics of Research Involving Pregnant Women and Fetuses

Adverse Events

Advanced Review of Adverse Events

Clinical Trial Protocol

The Clinical Trial Protocol - Advanced Mastery Review

Inclusion and Exclusion Criteria in Clinical Research (Writing, Assessing for Broad vs. Narrow, Organ Dysfunction, Older Adults, Pediatrics, Pregnant Women)

Protocol Deviations and Violations

Protocol Deviations and Violations (Major, Minor, Exceptions, Resolution)

IRB and DSMB

Institutional Review Board/Ethics Committee (IRB/EC) (Requirements, sIRB, Application, Exemptions, Expedited Review, Continuation, and Reporting)

Data Safety Monitoring board- DSMB

Review Questions

REVIEW: Review Questions for ICH GCP (for study purposes, not graded)

Site Monitoring Visits

Types of Monitoring Visits (Selection, Initiation, Routine, Close-Out)

Site Qualification Visit (SQV)

Site and Investigator Selection Criteria (Process, Criteria, Investigator Selection, Agreements, Decision-Making)

Site Selection/Qualification Pre-Study Visit (SSV/SQV) (Before, During, After, Letters, Checklists, and Report)

Site Initiation Visit (SIV)

Site Initiation Visit (SIV) (Before, During, After, Letters, Checklists, and Report) - Review from "Types of Monitoring Visits"

Routine Monitoring Visit (RMV)

Routine/Interim/Periodic Monitoring Visit (RMV/IMV/PMV) (Before, During, After, Remote, Letters, Checklists, and Report)

Site Close-Out Visit (SCOV)

Site Close Out Visit (Before, During, After, Early Termination, Letters, Checklists, and Report)

Tools for Monitoring Visits

Monitoring Tools and Softskills (Tools, Templates, Communication, Metrics, Motivation, Humanistic Qualities)

Develop Templates for Monitoring Visits (Site Preparation, Pre-visit Letter/Agenda, Visit Checklist, Followup Letter, Visit Report)

Audit and Inspections

Audits and Inspections in Clinical Trials

FDA Bioresearch Monitoring Program (BIMO)

FDA Warning Letter

Audits and Inspection Review Questions (for study purposes, not graded)

REVIEW A: Quality Monitoring Review Questions (for study purposes, not graded)

SDV and Informed Consent

ICH GCP Section 4.8 Informed Consent

Source Documents and Informed Consent Forms (SDV Checklist, Informed Consent Checklist)

Minimizing Source Data Queries In Clinical Trials

Case Report Form

Guidelines for Designing and Completing Case Report Forms

Do’s and Don’ts of a Case Report Form Design

Quality Control and Safety

Quality Control in Clinical Trials ( QC/QA, KQI, QMS, Checklist)

ICH GCP - Safety of Human Subjects in Clinical Research

Technology in Trials (IVRS, CTMS, EDC)

ICH GCP - Trial Management, Data Handling, and Record Keeping

Interactive Response Technologies in Clinical Trials (IVRS, IWRS, IRT, RTSM)

Clinical Trial Management System-CTMS

Electronic Data Capture and Remote Data Capture Basics

Electronic Regulatory Submission and Review

Modernized Monitoring (Remote, Risk-based, Centralized)

An Overview of Remote Monitoring - COVID-19 Update

Remote Monitoring of Clinical Trials and EMRs

Centralized Monitoring

Pharmacovigilance and Regulatory Affairs

Advanced Practice of Pharmacovigilance

Regulatory Affairs for Clinical Trials

Investigational Product

Investigational Product Storage and Dispensing

Investigational Product Accountability in Clinical Trials

Local and Central Labs

Local and Central Labs in Clinical Trials (Local, Regional, Central, GLCP, CLIA Cert, Lab Audit Checklist)

REVIEW PART B: Quality Monitoring Review Questions (for study purposes, not graded)

Regulatory Documents

Regulatory Documents in Clinical Trials

Delegation of Authority Log – DOAL

Investigators Brochure (IB)

CFR 21 Part 11 - Electronic Signatures

Code of Federal Regulations

CFR 21 Part 11

New Drug Application

The Investigational New Drug (IND) & New Drug Application (NDA) Process

Investigator Initiated Multi-Center Trials

IND and IDE AE Reporting

Safety Reporting Requirements for Sponsor Investigators of An IND

Trial Master File

Essential Regulatory Documents Binder Tab Organization (Trial Master File)

Trial Master File Reference Guide

Regulatory Training Quiz

Disclosures and Payments for PI, Site, Patients

Financial Disclosure- Duties and Strategies for Clinical Studies

Payments and Budgeting for Investigators and Site

Advertisement Aid in Subject Recruitment and Retention

Patient Recruitment, Retention, and Compliance

Patient Recruitment in Clinical Trials

Patient Engagement and Retention in Clinical Trials

Patient Adherence and Compliance in Clinical Trials

Misconduct and Fraud

Scientific Misconduct and Fraud

Detecting Falsification

REVIEW PART C: Quality Monitoring Review Questions (for study purposes, not graded)

Site Visit Templates

SQV Checklist

SQV Questionnaire

SQV Assessment

SQV Follow Up Letter

SIV Confirmation Letter

RMV Confirmation Letter/Fax

RMV Follow Up Letter

CRA TRANSITION Letter/Email/Fax

SCOV Confirmation Letter

SCOV Agenda

SCOV Report

SCOV Follow Up Letter

REFERENCE Module

Final Examination

Competency Exam

Start Today

• Monitor Trial Sites
• Preferred 4 Year Science Degree or RN License or Prior CRC
• Salary $60-120k+. High promotion rate.

CCRPS Reviews

Accelerated, zehra abbas.

Accelerated course but really concentrated. Practical and clearly explained. Perfect alternance of slides/lecture videos. Easily understandable by with histo...

Accelerated course but really concentrated. Practical and clearly explained. Perfect alternance of slides/lecture videos. Easily understandable by with history background and by other as well with thehelo of the slides.

Mary Dahodu

Great course with high knowledge impaction. Platform also was easy to navigate.

Dedication to real material

Asra feroze.

The diligence and direction provided by this course material has inspired my inner confidence to climb high to reach the pinnacle of my ambitions.

Refreshed my knowledge after 10 years in monitoring

Dr. sharib syed muhammad.

Best refresher for clinical researchers. A lot of content but can skim modules if you know them well.

a fundamental stepping stone for all monitors

George grudziak.

If you want to move up the ladder in clinical trials, this is the best course to take. It’s so affordable even though I’ve paid three times as much to learn ...

If you want to move up the ladder in clinical trials, this is the best course to take. It’s so affordable even though I’ve paid three times as much to learn what is covered in just a chapter. I refer back to the course every time I switch to a new trial to refresh my knowledge.

CCRPS trains monitors to succeed in remote and local site...

Esohe ayanru.

I was recommended to take the course by a friend who was transitioning to clinical trials. I had only worked in remote trials as a CRC before but wanted to m...

I was recommended to take the course by a friend who was transitioning to clinical trials. I had only worked in remote trials as a CRC before but wanted to move up. This course was so advanced and really made sure you understood all the core guidelines and monitoring report processes. It made me feel much more comfortable when applying for new jobs.

Phd In Monitoring

Adriana paz mancia.

Very practical given the potential scope of the material. The ability to cover so much material with examples is a real bonus and helps bring the content to ...

Very practical given the potential scope of the material. The ability to cover so much material with examples is a real bonus and helps bring the content to life through discovery and application. So many topics are covered almost like a bootcamp for phd in trials.This is helpful

two weeks to update your resume

Shivani dhotre.

CRA training took me about 2 weeks straight. I learned a lot and videos were very refreshing. It was noticed by recruiters on resume.

Detailed Information

Oladipo owoyomi.

This is one of the best courses i have ever done. Despite being online, the engagement was topnotch. Participation was of high standard and the knowledge, hi...

This is one of the best courses i have ever done. Despite being online, the engagement was topnotch. Participation was of high standard and the knowledge, highly inspiring. I recommend it for anyone with a research drive.

A great review of clinical research for monitors

Jayant shrivastava.

I found this course to be a very advanced, in-depth review of clinical trials. Absolutely everything you need to know is included in the course. There are lo...

I found this course to be a very advanced, in-depth review of clinical trials. Absolutely everything you need to know is included in the course. There are lots of templates in each module for SIV and other things which I really liked.

Learn by examples. Great follow through videos.

Abiodun adegbite.

Exceptional information not found anywhere else. Everything has an example. Content just makes sense as dry as reviewing protocols and guidelines can be.

Lifechanging for my career

Latoya munroe.

The work load of modules are much but through the video lectures and the pdf materials it became very easy to understand and assimilate. It a great experienc...

The work load of modules are much but through the video lectures and the pdf materials it became very easy to understand and assimilate. It a great experience as I was introduced to Clinical Research Associate Certification. Hoping to build a career through this. Awesome experience

How to become a clinical research associate

To become a clinical research associate, you must first complete an accredited clinical research associate training program. The course provides an extensive review of the regulations and principles of clinical research, as well as practical application of the skills needed to execute and manage trials correctly.

• Clinical research associate certification test covers topics like clinical research protocols, FDA regulations, Good Clinical Practice (GCP), ICH guidelines, data management and more. If you pass the exam, it means you're certified as a CRA.
• You can get clinical research associate training online free with webinars, tutorials, eBooks and other materials related to the profession. This can help you learn more about the job before you get certified.

A CRA makes sure clinical trials are done correctly and on time. They make sure the clinical trial follows the plan, good clinical practice guidelines, ethics, and laws. CRA's must know a lot about trial protocols, patient safety, data integrity and regulatory requirements to guarantee the quality of a clinical trial.

A clinical research monitor will review study sites' data collection processes to ensure that all data collected is complete and accurate. This includes conducting on-site visits to assess study sites' compliance with good clinical practices (GCP), review case report forms (CRF), and periodically audit research sites to ensure compliance.

Clinical research associates do things like teach the protocol; talk to human subjects and their families; get ready for investigator meetings, trainings, documentations; manage study supplies inventory; track subject enrollment, visits, data reports, study timelines; and solve any problems that come up during the study.

Clinical research associate certification

Getting certified as a Clinical Research Associate (CRA) gives you the opportunity to start earning salaries of up to $100,000 and 33% of new CRAs receive promotions within the first year.

The ACRAC training program is internationally accredited by industry standards including IAOCR, ACCRE, AMA, ACPE, ANCC to provide comprehensive training for those holding at least a BA in Science.

Flexible online training and on-demand video modules that can be completed in as little as 2 weeks for a clinical research associate fast track career.

Advanced clinical research associate certification through a highly regarded training program like CCRPS gives you the skills and knowledge to have an edge over other job seekers who are not yet advanced certified.

Clinical Research Associate Salary

Clinical research associate salary (CRA) is typically higher than the national average and varies depending on experience, job title, city of employment and industry. The average annual salary for a CRA was estimated to be $80,000 in 2024.

• Entry-level clinical research associate salaries can range from $47,000 - $80,000 per year. As a CRA gains more experience and furthers their education, they may be able to negotiate higher salaries due to their valuable knowledge and skills.
• Salaries for experienced CRAs can exceed $90,000 in certain geographies or with specialized skillsets. Generally speaking, the higher the level of education or specific certifications held by a CRA, the higher salary they can expect to earn.
• Various factors impact how much a CRA can earn such as their employer’s size and industry sector (pharmaceuticals vs biotechnology companies), amount of travel required for research responsibilities and tasks assigned.

What does a clinical research associate do

The Clinical Research Associate is responsible for creating clinical research protocols and Case Report Forms. This includes writing instructions, outlining procedures, collecting data, assessing collected samples/specimens, and making sure people follow the protocol/investigational plan.

The CRA role includes making sure that sites are monitored, data is accurate, and reviewing source documents. They also manage a team of physicians, nurses, support staff (if applicable), vendors (such as laboratories) involved in the clinical trial and providing training on protocol requirements in order to achieve successful outcomes from each trial/study conducted.

CRAs need to make sure they follow all the rules and regulations for conducting studies. This includes making sure the studies are safe for patients, ethical, and accurate. CRAs also need to attend regular meetings with people who are involved with the study to discuss any changes in the rules or regulations that could affect how the study is conducted.

Clinical Research Associate Jobs

Utilize online job boards, such as Indeed and Glassdoor, to search for open positions. When searching, use keywords such as "clinical research associate jobs", "clinical research associate job", "clinical research associate jobs entry level" and "remote clinical research associate jobs". Make sure to write a cover letter.

• To find potential employers as a Clinical Research Associate, look in directories of medical companies or local businesses.Contact the employer by email or phone and tell them why you would be good for the job they are trying to fill.
• Talk to people who have jobs like the one you want, follow professional organizations on LinkedIn, and go to events where you can meet these people. This way, you might hear about job openings.
• Check social media for job postings by following accounts related to Clinical Research Associates and checking them regularly for new postings that might be a good fit for you.

Clinical Research Associate Certification FAQs

Clinical research associate course syllabus.

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The CRA Training Institute

Training & Onboarding Clinical Research Professionals since 1989

Online cra, crc & cdm clinical research courses .

 Receive your Accredited Certificate and be

job-ready in as little as 3-4 Weeks! 

CRA Certificate Course

COURSE FEE:     $79 9.00

DURATION:      3-4 Weeks Average

                          No Time Limit

DELIVERY:       100% online

                          Self-Paced Stu dy

START DATE:     Immediately

CRC Certificate Course

COURSE FEE:     $74 9.00

DURATION:      2-4 Weeks   Average

                          Self-Paced Study

CDM Certificate Course

COURSE FEE:     $6 9 9.00

DURATION:      2-3 Weeks

DELIVERY:       100% o nline

Trusted by CROs & Biotech Companies Globally

Curavit Clinical Research

Accreditation

The cra training institute and its online clinical research courses are accredited by the accreditation council  for clinical research education (accre)..

Global Program Code

463-04-112-GPC02

www.accre-accredit.org   1840 W Whittier Blvd #4320 La Habra, CA 90631 USA Phone: 1-(888) 512-6760

Student Testimonials

Got hired as a pharmacovigilance officer for IQVIA working with Moderna on their Phase III mRNA vaccine candidate! Thanks so much for your help.

S. Ray, MD, MSc, CRA - Georgia

Job placement assistance.

Professional Resume preparation

Interview preparation

Connecting with Employers

Our Alumni have either found employment with or have been referred from a wide cross-section of hospitals, clinics, CROs, biotech and pharmaceutical companies across North America and globally.

With the knowledge and job skills gained as a result of your study, you can help to meet the ever-growing demand for trained CRAs, CRCs or CDMs to develop exciting new therapeutics for the 21st century in the biotechnology, pharmaceutical and medical device industries.

Clinical Trials in a Nutshell

Our Accredited Interactive-Online Clinical Research Courses are designed for persons with or without prior on-site clinical trials monitoring experience, seeking qualifications and/or current practical knowledge to effectively work as a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), or Clinical Data Manager (CDM) in the monitoring of clinical trials globally.

Online CRA, CRC & CDM Clinical Research Courses

Register Now

Once registered, we will add you to our CRA Academy list and reach out to you soon to collect your payment details. We accept credit/debit card payments only.

For more information contact:

[email protected]

Next class starts april 2024.

The only Clinical Research Academy that provides practical, real industry experience for future clinical research associates, coordinators, and dozens of other positions.

NOW OFFERING ONCOLOGY MONITORING EXPERIENCE remotely to students who successfully graduate!

Students Acceptance Per Quarter

Pedagogical Staff Support & Educational

Online Resources E-Learning, eTMF, EDC

Educators : Students Ratio (+ Surprise Guests)

Working Graduates Since 2016

NEXT QUARTERLY SESSION BEGINS THE WEEK of

April 14, 2024.

This training applies to most clinical research positions such as CRAs, study coordinators, and dozens of other industry roles! We are proud to announce that we now offer oncology experience for our internship component for students who successfully graduate. We also support full remote monitoring internship opportunities for this indication!

We help our students to:

• Understand the fundamentals of clinical research from the perspective of a generalist
• Gain industry experience after passing the 3 month online course with an optional onsite internship (exceptions apply) or remote internship which is always included
• Practical job interview preparation, job lead recommendations, and CV preparation that will make a difference.
• Unlimited support throughout your clinical research career
• Obtain Oncology as well as other therapeutic indication experience

How The Academy Is Structured

The CRA Academy is a 3 month course that has an optional and free remote internship program where students who successfully complete the three month course (score a cumulative grade of 80% or higher) will be given the opportunity to gain valuable industry experience while working on real studies.

Our academy is 100% online with weekly video modules followed by a weekly live webinar taught by one of our CRA instructors. The 1 hour webinars are held every Saturday at 1 PM PST for the duration of the academy. During the webinars, the lessons from the prior week’s module will be reviewed, questions will be answered, and homework will be assigned. We use real virtual workspaces and actual EDC systems that are used in the industry in order for students to better familiarize themselves with common industry tools.

After the 3 month academy, a final exam will be given and students must pass the exam to successfully complete the academy. During the 3 month course students will also become GCP and IATA certified. Post-academy internships will be made available for everyone who successfully completes the 3 month training.

After successfully completing the course material, students have the option of doing internship activities remotely (online), or at a site near them (exceptions apply), or a combination of the two. There is no additional fee for either of these options and we have seen that students who take advantage of these free opportunities tend to land industry positions faster.

Additionally, we are wholly owned by DSCS CRO which engages in phase 1-4 industry sponsored and investigator initiated trials. Some of our trials on clinicaltrials.gov can be found here , here , and here . Students will be given opportunities to work within our CRO on the above linked trials during the internship phase, and any student that participates in our online internship will have an opportunity to monitor an oncology project that our CRO manages. Certificates will be distributed to students who have successfully completed the coursework.

Why Be A CRA?

CRAs are always in high demand and the career can be quite rewarding. There are however, very few opportunities out there for individuals without any knowledge or industry experience. The minimum requirements for an individual to become a CRA are as follows:

• Prior industry experience is typically required
• Must have at least a Bachelor’s degree (foreign degrees are acceptable; degrees do not have to be science related)
• Must have a working knowledge of the fundamental principles of clinical research

Claud & Lora

Marchna & Reploly

Emanuel, Lucky & Angelica

We are a group of individuals that have been operating various clinical research sites, CROs, and consulting companies since 2005. Due to a huge demand, from many of our clients, we have decided to create The CRA Academy as a tool for not only teaching the fundamental principles of clinical research, but also to provide students with some much needed (and often required) industry experience.

Tiffany Bennett

Chris Sauber

Prior to entering the clinical research industry, I graduated from the University of Southern California in 2005 with a Bachelor’s degree in Health Promotion and Disease Prevention Studies. In 2013, I obtained a certificate in Pharmaceutical and Healthcare Business from the University of Sciences, Philadelphia.

In my career, I have worked for private practices, major pharmaceutical companies and clinical research organizations as a data manager, clinical project coordinator and clinical research associate. I was a Site Director for a physicians network for clinical trials and I currently hold the Director of Clinical Research position for the Ora Lee Smith Cancer Research Foundation (a non-profit organization aimed to eradicate solid tumor cancer cells with a laser medical device, more specifically a Laser Activated Nanotherapy Technology). I also had the opportunity to teach multiple medical doctors and over 50 pre medical students the basics of clinical research for the National Medical Association.

I have 16+ years of experience as a clinical research professional and I have helped hundreds of individuals enter the clinical research industry.

Dan has owned and operated clinical research sites since 2005 when he learned to become a clinical research coordinator on his own. Since that time, Dan has worked as a contract CRA in addition to being Site Director and a consultant to the life sciences industry.

Chris started out in clinical research as a study coordinator and quickly transitioned into a CRA, project manager, auditor, contracts and budgets specialist, site director, site owner, CRO co founder, amongst other roles that have made him an all around generalist in the industry.

Frequently Asked Questions

How long is the internship.

The internship is only available to students who pass the final exam. We typically recommend graduates spend at least 3 months for the internship phase however students may intern for as long as they need in order to gain the necessary work experience. We do not charge anything extra for the internship.

Can I do the internship remotely?

Yes. Although we recommend everyone try to intern at a research clinic near them (exceptions apply), most monitoring activities, such as source data verification and source data review, can be accomplished remotely. Furthermore, to guarantee that students gain oncology experience, they must participate in the remote internship.

Do I need to quit my job to intern?

No. We purposely limit your workload to no more than 6 hours per week and interns can make their own schedule for the most part.

Are We Accredited?

While we have been accredited in the past, we chose to not renew our accreditation due to the fact that we operate as a CRO and Site Network and employers much prefer our real study experience opportunities for our interns rather than an arbitrary accreditation.

FREE 4.5 hour comprehensive crash course of many of the topics we cover.

Have a question.

To learn more about The CRA Academy, please fill out the contact information below:

MOBILE NUMBER

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Enrollment Cost:

$5,000 usd per student, tuition fee includes 3 month online classes, materials and internship..

We accept credit/debit card payments only. You may register now if you'd like. Fill in the fields provided on the sidebar of this website with your first name. last name, email address, and mobile number and press the “Register Now” Button.

Once registered, we will add you to our CRA Academy list and reach out to you soon to collect your payment details. We accept credit/debit card payments only

Special Circumstances:

If necessary, the class can be paid for in two installments of $2,500. The first payment is due upon registration and the second payment of $2,500 will be due during the second month of the program.

NOTE: A BACHELOR'S DEGREE IS REQUIRED TO BE EMPLOYED IN THE RESEARCH INDUSTRY AS A CRA

Cancellation policy.

Once access to the course has been granted, there will be no refunds. If a student for some reason is unable to complete the quarter, we can make arrangements to place them in the following quarter's class.

"The CRA Academy" is owned and operated by DSCS Sweat Equity & Investments, LLC & The Clinical Trials Guru, LLC

T: (949) 415-6256 | E: [email protected]

1830 Commercenter East San Bernardino, CA 92408

• What Is Clinical Research
• Introduction
• The Role And Responsibilities Of A Monitor Per Fda And Ich-gcp
• Pre-study Visit
• Site Initiation Visit
• Interim Monitoring Visit
• Close Out Visit
• In-house Cra Roles And Responsibilities
• Coaching/Mentorship (1hr)
• Interview Session Nov 2021
• Interview Session With Ronke 01 jan 2022.
• Interview Session 29 Jan 2022
• Group Interview Session 26 Feb 2022
• 3 Months Subscription Plan
• 6 Months Subscription Plan
• 1 year Training Program

Welcome To THE CRA SCHOOL

Clinical research associate start-up kit.

CRA START UP KIT

The Clinical Monitor's Planner

Our pricing.

Pre-Recorded live sessions

EDC and IWRS demonstration

How to review regulatory documents

How to review eTMF/ISF

How to perform drug accountability and reconciliation

How to properly prepare for interviews

Understanding and learning to incorporate keywords

Entry-level jobs and requirements

ICH-GCP/FDA Training Standard

All training content provided in this training videos are in accordance with ICH-GCP and the FDA. We follow all principles and guidelines provided by all clinical regulatory bodies, as applicable.

One On One Coaching

We offer one on one coaching after you have reviewed the videos to ensure all questions are answered to your satisfaction.

On The Job Mentoring And Support

We offer the support needed to transition from new-hire to stellar employee. We provide support for unfamiliar scenarios and provide the best course of action to yield the best outcome for patient safety and the sponsor.

Interview Preparation

During this phase, we go through intense clinical research scenarios and help you resolve them, not only for the interview but for longevity. The goal is to ensure that you always understand the “why.”

Crisis Management In Clinical Research

As crisis is a typical part of the job, it is essential that we provide excellent crisis management tools and steps to ensure you are performing at your best.

Tools Of The Trade

We offer various tools for a select membership type. These include monitoring plans, monitoring checklist, remote ISF checklist, SIV checklist, COV checklist, SDV tracker/Planner, Subject visit tracker/planner, etc.

How It Works

Select a Plan

Start Training

Frequently asked questions, what does my training cover.

Please refer to the pricing page

Do you review and rework CVs?

No! I do not; however, I give you tag words that will help your CV be visible.

Can we request additional 1:1 time?

Yes you can, but priority is given to members based on their status (for additional coaching only.)

How much time do I need to get trained?

It depends on your pace, but to be comfortable enough to interview, you need to know what you are talking about and there is a lot of content to cover.

Have a Question?

• Login / Register

ACRP Course Catalog

Refine Results:

Knowledge level:.

• Entry Level
• Intermediate

CATALOG GROUPS:

• In-Person Training
• Webinar Replays
• Recorded Conference

COMPETENCY:

• Clinical Trials Operations and GCPs
• Communication and Teamwork
• Data Management and Informatics
• Ethical and Participant Safety Considerations
• Leadership and Professionalism
• Medicines Development and Regulation
• Scientific Concepts and Research Design
• Study and Site Management
• Clinical Study Operations

PRIMARY ROLE:

• CTMS Administrator
• Clinical Research Nurse
• Business Development
• Clinical Research Scientist
• Clinical Data Coordinator
• Billing Compliance Officer
• Clinical Research Coordinator
• Data Manager
• Director of Pharmacovigilance
• Director of Scientific Affairs
• Director or Manager of Clinical Trial Operations
• Director or Manager of Regulatory Affairs
• Drug Safety Manager
• Drug Safety Physician
• Financial Analyst
• Investigator
• Medical Affairs
• Medical Director
• Medical Research Scientist
• Medical Safety Officer
• Medical Writer
• Monitor or Clinical Research Associate
• Patient Recruiter
• Project Manager
• Quality Control Specialist
• Regulatory Specialist
• Research Manager
• Research Technician or Assistant
• Site Selection and Start Up
• Statistician
• Sub-Investigator

107 results

For Individuals

For Business Partners

• Entry Level , Intermediate , Senior

The Future of Home Health Care in Clinical Trials

May 22, 2024—This live session will provide insights into the presenters experience with home health visits to-date and will prompt site and investigator attendees to understand what works and doesn’t work for sites when offered home health options in trial protocols.

Contact Hours

From Conflict to Collaboration: Enhancing Site and Sponsor/CRO Relationships

June 12, 2024—This live webinar delves into the perspectives and occasional conflicting interests of both parties, fostering mutual understanding. Representatives from each organization will share insights, real-life examples, and practical tools to overcome challenges, promote productive collaboration, and contribute to clinical trial success.

ACRP and the Academy Annual Membership Meeting

October 16, 2024—Join ACRP and the Academy leadership to explore highlights of ACRP’s year and what’s planned for 2025.

Employee Development and Succession Planning

This webinar targets site and organizational leaders with the kinds of details they need to pay attention to in order to develop the framework for an employee development program which will support succession planning.

Intro to In Vitro Diagnostics (IVDs): The Path to Working Together Globally and More Efficiently

This webinar addressed the pressing need for standardized regulatory practices in the field. With advancements in in-vitro diagnostics (IVD), an increasingly interconnected global healthcare landscape, and the growing demand for precise diagnostics, the need for harmonized regulations is paramount.

Clinical Trial Process History and Overview

This webinar covered phases of drug development, the history of regulatory development of human research protection, various types of research study designs, conducting a clinical trial, and generic name and trade name of the medicine.

Efficiency Unleashed: Optimizing Clinical Research Onboarding and Education

Clinical trial professionals with an interest or role in the onboarding and education of new staff can learn valuable best practices from the steps taken, barriers encountered, and resources available during one clinical trial site’s journey toward realizing its goal for optimal efficiency.

Building Your Team Through Transformational Leadership in Clinical Research

This webinar challenged attendees to self-reflect on their own leadership practices and how those might have been in need of transformation

ISO 14155 and FDA Requirements – Trials Conducted at the Research Site

This program explored medical devices and investigational medical devices.

Unlearn to Learn: The Evolution of Clinical Research/Trial Training

This session discussed the current way clinical trial training is implemented and ways that it could potentially be done more effectively and efficiently by industry stakeholders.

A Review of Medical Record Data Extraction and Adverse Event Reporting

This informative session explores some of the tools of the clinical research trade including data extraction and adverse event reporting.

Broadening Your Approach to Trial Diversity on a Global Scale

This live webinar explored diversity through a global lens by tapping into the perspectives of industry leaders who addressed how we can broaden access to a wide range of underrepresented groups, including those who possess attributes linked to troubling and challenging health disparities.

Merck Journeys: Elevating your Career within Clinical Research

This webinar offered a unique opportunity to learn about the rewarding career paths in CSSM. Experienced professionals from Merck shared insights into the innovative clinical research strategies, and discussed how your transferable skills can be leveraged in this field.

ACRP Annual Membership Meeting

ACRP and The Academy leadership joined together to explore highlights of the past year and see what was planned for 2024. Attendees heard how ACRP is working for them and the clinical research profession.

Investigator-Initiated Trial Tips and Tricks

This webinar highlighted best practices in various areas of clinical research management of investigator-initiated trials (IITs) and detailed how to navigate common challenges. The information included in this comprehensive review of IIT operations is experience-based and built upon good clinical research practices in alignment with NIH Regulations.

Good Clinical Practice (GCP) Simulation Renewal

The New Standard in GCP Training. This interactive simulation-powered training course helps ensure compliance with international standards for Good Clinical Practice in clinical trials (ICH E6).

Home Study: August 2023

Supplement more rigorous training, stay informed of the latest trends and developments in clinical research, and earn points for Maintenance of Certification with Home Study tests offered through ACRP’s flagship journal, Clinical Researcher.

• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, , Trainer

Introduction to Decentralized Clinical Trials (DCTs)

Gain the foundational knowledge clinical research professionals need to implement digital health components in clinical trials.

Investigational Drug Services Pharmacists: What They Wish You Knew

How the Investigational Drug Services (IDS) Pharmacy utilized by your clinical trials team works shouldn’t be a mystery, when it can instead be one of your biggest allies in research. This webinar provides “insider insights” from an IDS pharmacist on facts you should have at hand about IDS services when sponsors are considering your site for studies, or are sending monitors to keep track of ongoing projects.

How Do IRBs Review Virtual Trial Technology?

How will institutional review boards (IRBs) review study protocols involving the ever-increasing array of mobile health (mHealth) technologies and virtual trial apps on the market? This webinar helps clinical research professionals to understand the regulations and how the oversight of virtual trials might differ from what they have traditionally been used to.

Home Study: June 2023

Acrp 2023 full program – replay.

A replay package of 62 on-demand session recordings and presentation slides from the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. It includes content from the five educational tracks, the Signature Series sessions, Rapid-Fire session, and techXpo sessions, presented by a variety of clinical research service providers. Replay sessions will expire on May 31, 2026.

ACRP 2023 Workforce Development – Replay

This package is a replay of 8 on-demand session recordings and presentation slides from the Workforce Development Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Understand the workforce landscape and gain strategies to build smarter teams.

ACRP 2023 Technology & Future Trends – Replay

This package is a replay of 7 on-demand session recordings and presentation slides from the Technology & Future Trends Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Gain strategies to optimize technology and move your studies into the future.

ACRP 2023 Leadership & Career Growth – Replay

This package is a replay of 10 on-demand session recordings and presentation slides from the Leadership & Career Growth Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Get the insights you need to advance your career and grow as a leader.

ACRP 2023 Regulatory Trends & Compliance – Replay

This package is a replay of 10 on-demand session recordings and presentation slides from the Regulatory Trends & Compliance Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Hear tips and strategies to mitigate risk and keep your studies in compliance.

ACRP 2023 Study Management & Conduct – Replay

This package is a replay of 17 on-demand session recordings and presentation slides from the Study Management & Conduct Track at the ACRP 2023 Conference, April 29 – May 1, Dallas, Texas. Learn practical, proven ways to maximize study and site performance.

Home Study: April 2023

2022 site perceptions industry survey results: actionable insights for sites, sponsors, and cros.

Site leaders often feel their voices are not heard during the planning and conduct of sponsored clinical trials, while sponsors and contract research organization representatives feel at odds struggling to enhance relationships with those same sites. This webinar focuses on the results of an industry survey conducted by the Tufts Center for the Study of Drug Development on site perceptions, preparedness, and experiences with new clinical research execution solutions, and offers lessons learned on how you can improve site sustainability and lead more effective collaborations.

I Need a Mentor: Where Do I Start?

Career success shouldn’t be measured solely by how far one is able to climb the organizational ladder, especially when reaching career goals depends on so much more than mere effort. In an environment where achievement may rely less on “what you know” than on “who you know,” identifying the right individuals to be part of your knowledge bank and support squad can become crucial.

Building a More Equitable Future Together by Driving Inclusion in Clinical Trials

This webinar targets professionals across the clinical trial ecosystem with best practices learned about taking collective action to drive improvements focused on diversity, equity, and inclusion (DEI) issues. You will learn about building trust within historically underrepresented racial and ethnic minority communities, making clinical trials inclusive by design, and fostering partnership to address DEI-related issues in an integrated and sustainable manner.

Building Clinical Trial Diversity Action Plans for the Future, Now

Dive into the key elements of a diversity action plan for Phase III clinical trials, as explained in the latest recommendations and requirements from the U.S. Food and Drug Administration (FDA), including considerations of race, ethnicity, age, sex, gender, geographic location, and socioeconomic status. Learn how these diversity action plans contribute to the study site’s delivery of meaningful data on drug safety and efficacy from to sponsors.

Home Study: February 2023

Home study: december 2022, a review of ich e8 (r1) general considerations for clinical trials.

The ICH E8(R1) Guideline on General Considerations for Clinical Studies from the International Council for Harmonization guides the clinical development lifecycle for experimental therapies, including quality requirements for clinical study designs and data sources. Principles and practices for the conduct of clinical trials tied to this guideline, already in effect in such regions as the U.S., Canada, and Europe and forthcoming elsewhere, will be reviewed.

Achieving Global Health Equity Through More Diverse and Inclusive Trials

Ensuring a more equitable and accessible healthcare system starts with the healthcare professionals engaged for pre-drug launch and marketing, with the site investigators recruited by sponsors to run clinical trials, and with the location and availability of the study in terms of diverse and underrepresented populations of potential participants. Here’s a historic overview of what has been lacking in clinical trials when it comes to diversity and inclusion, how federal guidelines are beginning to turn the conversation within big pharma toward health equity, and more.

2022 ACRP/Academy Annual Membership Meeting

Join ACRP/Academy leadership to explore highlights of ACRP’s year and what’s planned for 2023 in the areas of membership, certification, and finances.

Home Study: October 2022

Self-leadership: winning strategies for fulfilling work and life (part 1): theoretical foundations and core competencies of self-leadership.

Learn how to use self-leadership strategies to survive and thrive in today’s volatile, uncertain, complex, and ambiguous world.

Ensuring Quality in Fast Enrolling Trials

Are new trials coming at you with break-neck speed? This webinar reviews a case study from a fast-enrolling trial and offers strategies for maintaining high quality standards and recognizing and mitigating the risks of accelerated enrollment.

Webinar—Self-Leadership: Winning Strategies for Fulfilling Work and Life (Part 2)

Learn even more about using self-leadership strategies to survive and thrive in today’s volatile, uncertain, complex, and ambiguous world, in part two of this webinar. 

In the DCT Journey, Every Cloud Has a Silver Lining

This webinar focuses on some of the advantages and takeaways learned so far from the introduction, implementation, and adoption of decentralized clinical trials (DCTs). Panelists explore how they operationalized best practices in the areas of budgeting, contract language, remote monitoring practices, virtual visits, and more.

ICH E9: A Review and a Look Into the Addendum (R1)

Dive into an overview of both the ICH E9 Guideline on Statistical Principles for Clinical Trials from the International Council for Harmonization and the ICH E9(R1) Addendum, exploring how clinical trials are based on statistical principles and how treatment effects are measured.

Understanding the Role of DMCs and EACs in Research Oversight

Take a deep dive into the roles and functions of Data Monitoring Committees/Data Safety Monitoring Boards (DMCs/DSMBs) and Endpoint Adjudication Committees/Clinical Events Committees (EACs/CECs) in the lifecycle of clinical trials. These committees are increasingly tasked with providing independent, expert evaluations of clinical trial events and unbiased adjudications to determine if the definitions of certain clinical trial events have been met.

Everything You Need to Know About Holding an IND

This webinar provides a review of the purpose of and expectations set for holding an Investigational New Drug (IND) application through the U.S. Food and Drug Administration, explores common IND-related errors and how to avoid them, and outlines related requirements found in 21 CFR 312 of the Code of Federal Regulations for IND maintenance.

Deconstruct Your Clinical Trial to Plan a Positive Outcome: Effective Planning and Communication Strategies

This webinar examines the communication of intent and expectations to stakeholders in clinical trials to minimize risk and gain fluidity in operations, along with key elements behind planning a clinical trial and best practices for budgeting a study.

Streamline Your Clinical Research Organization’s Processes with End-to-End Promotions

Presenting a discussion on how consolidating the processes involved in the phases of drug discovery, pre-clinical research, clinical trials, and post-approval expectations on a single platform drives efficiencies, margin improvements, and real-time collaborations internally and externally. The result is better top- and bottom-line financial performance and consistency in process outcomes during trial execution.

Best of ACRP 2022

The “Best of ACRP 2022” package offers recordings from 25 of the most popular sessions from our most recent in-person event, along with seven techXpo sessions, presented by a variety of clinical research service providers.

Eliminating Barriers to Careers in Clinical Research

A perfect storm of negative trends is putting immense pressure on entry-level hiring, retention, and overall satisfaction and growth in the clinical research workforce. This webinar focuses on recognizing and overcoming the challenges that are unnecessary barriers to greater participation in the workforce by promising talent from a range of backgrounds and experiences.

The New Work Life Balance in Clinical Research

There’s no denying that “work as usual” has gone out the window in recent years–in the clinical research workforce as well as in most other settings. This webinar explores strategies for juggling a career in clinical research and your personal life in the “new normal,” including in the arenas of excelling at time management in the office and at home, reaching an ideal work/life balance, and acquiring tools to help make your goals a reality.

Virtual ACRP 2021 Full Program Replay

ACRP 2021 programming delivers practical strategies, best practices, and creative solutions needed to improve clinical trial quality.

Virtual ACRP 2021 Innovation in the Era of COVID Track Replay

Unlock your potential by learning innovative new ways clinical research is being conducted in response to COVID-19. This online, interactive program addresses telemedicine, remote monitoring, team management, study start-up and more in the era of COVID.

Virtual ACRP 2021 Regulatory Trends & Compliance Track Replay

Mitigate risk and improve regulatory compliance with insider advice from FDA officials and industry experts. This online, interactive program features FDA officials and industry experts addressing CDER BIMO compliance and enforcement, FDA inspections, ClinicalTrials.gov requirements, and more.

Investigative Site Diversity: Tufts CSDD Study on Staff Diversity at Clinical Research Sites

In this webinar, the Tufts Center for the Study of Drug Development team shares survey results on staff diversity at clinical research sites, with an emphasis on the impact diversity has on site performance and its practical implications, the major factors noted for diversity-related success and their associated barriers, and the relationship between site diversity and patient diversity.

The Push for Technology: A Discussion of Implementation Struggles, Strategies, and Lessons Learned

This webinar features a panel discussion on how the pandemic pushed the implementation of new technologies for clinical trials, with a site-centric focus on the struggles overcome and lessons learned, along with the impact on the workforce and how we all may want to prepare for the future.

Best Practices for Communicating Benefit, Risk, and Uncertainty in Medical Device Clinical Trials

This webinar focuses on how research participants cannot make an informed decision to participate in a clinical trial without clear communications from the research professionals supporting the trial. Evidence-based practices are covered to help you conduct patient education and informed consent tied to the benefits, risks, uncertainties, and patient preferences for using new medical technologies.

Using Agile Strategies to Solve Challenges in Research Operations

This webinar looks at how being agile in research settings is becoming a key performance indicator that partners and sponsors are seeking and expecting from sites, with a focus on techniques and strategies you can use to address and solve administrative and operational challenges at a faster rate via pragmatic and thoughtful “big swings of bold.”

Virtual ACRP 2021 Operational Efficiencies Track Replay

Boost efficiency in clinical trial management and execution with practical strategies for sites, sponsors, and CROs. This online, interactive program addresses collaboration, protocol feasibility, decentralized trials, remote monitoring, and more.

Clinical Research Staffing Reprioritizations and Resourcing Strategies

This webinar presents lessons learned from a survey on the impacts of the pandemic on staffing at research sites, and discusses implications for the future of clinical research workflows from the current shift to remote operations. When should you look for help or change your staffing approach?

The Future of DCTs: Are You Prepared?

This webinar is tailored for research professionals in sponsor, contract research organization, and study site settings who wonder how to embrace the challenges and benefits of decentralized clinical trials (DCTs), and includes a practical guide for what DCTs really are, how there is no going back, and how it is up to the research professional to adapt to change.

Research Ready: Leveraging Technology in the New Research Landscape

Join Advarra experts in a discussion on how to leverage technology in the new research landscape

Working with Site-Based Paperless Solutions and Ensuring Audit Readiness

Join RealTime experts for an overview of site-based electronic systems that the research industry is rapidly adopting.

Achieving Regulatory Compliance via Collaboration: Technology and Site Perspectives

Join experts from WCG Velos and the University of Kansas Medical Center to learn top practices and processes sites follow to meet compliance standards.

Communication Strategies for Conflict Resolution in Clinical Research Teams

This webinar examines group dynamics, team function, and how conflicts arise within the research team, and considers how specific communication behaviors can foster effective conflict resolution that facilitates team growth.

Career Paths in Clinical Research: Sharing the Journey and Providing Insight

Join a panel of clinical research professionals as they discuss their career paths into and through the clinical research industry, consider the future of their roles, and share advice with those wanting to join the industry. You will gain an understanding of the different research roles, areas that are ripe for career growth and development, and how you can prepare to thrive amidst future trends.

Let’s Talk Patient Recruitment: Strategies, Tools, Communication

This webinar reviews two participant recruitment strategies with guests who have helped increase efficiencies and increase recruitment into clinical trials. Be prepared to walk away with some new tips and tricks that you may be able to implement into your recruitment strategy as well.

Clinical Trial Diversity: Strategies to Support Patients, Sites, and Sponsors

This webinar focuses on ideas for educational outreach to promote the purposes and value of clinical research within organizations and communities, and considers what measures sponsors and sites can take to engage diverse patients in their clinical trials.

Monitoring Investigator-Initiated Trials

This webinar offers organizations valuable knowledge regarding how to create a process for internally monitoring the quality and safety of investigator-initiated trials. Templates, workflows, and other tools are shared so that learners may adapt the proposed program to their own institutional needs.

Improving Technology Proficiency in Clinical Research

This webinar considers how sites are shifting away from sponsor-provided systems into technology that meets their business needs. As the options for technology solutions continue to grow, research sites must develop a true technology strategy and develop proficiencies in selecting, implementing, maintaining, and connecting their technology.

How to Build Advanced Workflows with an Integrated Technology Environment

Join Florence Healthcare to learn how to harness the power of best-in-class software while avoiding digital fatigue, duplication, and wasted time.

Quality Improvements as a Result of Paperless Site-Based Systems

Join RealTime CTMS to examine how paperless sites and site networks are driving quality and improved timelines for the clinical research industry.

Exit the Feature Battle: How to Think Long Term and Prepare Your Site for the Future of Technology in Clinical Research

Join Veeva Systems to explore the key qualities and features sites need to look for in their technology partners to increase their connectivity with sponsors and patients.

Research and Expanded Access in Pandemic Times

This webinar provides an overview of the mechanisms through which, in pandemic conditions, experimental COVID-19 therapies and diagnostics were made available to patients and providers before clinical trials had established whether those products were safe and effective. Also considered are how this state of affairs affected researchers’ ability to generate substantial evidence of product effectiveness through high-quality trials and the U.S. Food and Drug Administration’s deliberations over potential COVID-19 vaccines.

Good Clinical Practice (GCP) Simulation

Esource: why this is the platform of the future.

Join experts from Clinical Research IO to explore how several independent trends in research will make eSource a platform technology for sites.

The Impact of Brexit and COVID-19 on Clinical Research Data Processing in the EU/UK

Join The DPO Centre for this exploration of data protection challenges relating to the handling of sensitive personal data of EU and UK trial participants and how COVID-19 has bought data protection to the forefront of people’s minds.

Transforming SOP Infrastructure for COVID Times (Session II)

This second of two webinars on best practices in crafting standard operating procedures (SOPs) for clinical trials applies the concept of emotional quotient-based design thinking to appropriately draft SOPs that include all potential stakeholders. Also considered will be common blind spots within basic compliance mechanisms and the keys for drafting more adaptive SOPs to serve as reference tools and training materials for preparing your organization for new ways of conducting clinical trials.

SARS-Cov-2, the Law, and You

In this webinar, the Association of Clinical Research Professionals and the Society for Clinical Research Sites offer a collaborative discussion on how new laws and regulations arising from the COVID-19 pandemic conditions affect small clinical research sites.

COVID-19 Technology Mad-Dash, What Worked and What Didn’t?

This webinar addresses the challenges of transforming clinical research operations with technology built during the upheavals research sites underwent in the midst of COVID-19 disruptions. You will gain a better understanding of the technology evolution experienced by the clinical research enterprise, how best to future-proof operations to avoid future disruptions such as this, and tips for operating your site with a view of both short- and long-term goals.

Innovative Approach of Using EHR Data to Improve the Speed, Efficiency, Quality and Costs of Conducting Clinical Trials

This webinar describes how a research site’s electronic health record (EHR) data can be used to precisely identify potential subjects from its patient population, thus reducing recruitment and screening efforts and accelerating time to completion of enrollment. Involved are the use of eConsent to enroll patients from their homes, the collection and use of relevant real-world data extracted from the EHR in ways that eliminate certain study visits and manual data entry, and the use of eSource for cutting the need for source data verification.

Practical Tips for Career Development

This webinar describes techniques for developing yourself as a better leader, as well as tools for developing a strong team that fosters open communication and respect of different personality styles. It provides practical tips for developing career ladders for individuals who wish to grow, hints on how to be flexible in terms of your team’s work environments and scheduling, and lessons learned on how to interact with external teams in order to facilitate strong inter-departmental communications and work flows.

Building Relationships With Healthcare Professionals and Community Groups to Increase Enrollment

This webinar focuses on best practices for building and maintaining relationships with healthcare professionals and community groups to increase study enrollment, particularly among diverse patient populations. You will learn how to manage productive physician and community networks that result in highly qualified patient referrals through real-world examples of successful site efforts, and from recommendations on practical adjustments sites can make to their existing strategies to maximize their efforts without overburdening their schedules.

Diversity of Research Personnel: Knowing Who We Are to Know Who We Serve

This webinar highlights how lack of diversity in the recruitment of study subjects impacts the generalizability of research findings, and how evaluating diversity among your research team members will inform study design and recruitment strategies. In turn, this will increase diversity among recruited subjects and make research findings more broadly applicable to wider populations.

Informed Consent Simulation

This interactive, simulation-powered training program helps ensure informed consent is obtained by the right subject, with the right forms, by the right people, through the right process, at the right time, and with the right documentation.

ACRP Clinical Research Knowledge Assessment™ (CRKA)

Whether you’re an emerging professional looking to demonstrate your foundational knowledge to prospective employers or an organizational leader looking for an efficient, effective way to vet new hires, ACRP’s new Entry-Level Knowledge Assessment (ELKA) is for you.

Certified Quality Manager Training

Increase your influence and expand your career opportunities by validating your commitment to quality. The Quality Management Institute and ACRP have partnered in a program of education for individual professionalism and the quality management of clinical research sites.

• BCO, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, PMs, QCS, RS, RM, RTA, SSSU, Statistician, , Trainer

Clinical Trial Monitoring Basics

Become an expert on quality and risk-management strategies and procedures. This interactive eLearning course answers the fundamental questions: What is RBM and how is it different from the standard monitoring approach?

• Entry Level , Intermediate
• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, , Trainer

Ethics and Human Subject Protection: A Refresher Course

When in need of a comprehensive refresher, this on-demand eLearning course provides a consolidated overview on the history and importance of ethical conduct in clinical trials involving human subjects.

• Investigator,

Investigator Responsibilities

Learn the various responsibilities of clinical investigators based on FDA Regulations, ICH Guidance Documents, and international standards.

Improving Recruitment, Accrual, and Retention in Clinical Trials

Explore best practices to improve recruitment and retention with a focus on operational efficiency, cultural competency, and patient centricity. Included tools will help you assess how to better communicate with potential participants and begin a critical reflection of your own skills and organizational practices.

Trial Feasibility and Selection: Their Impact on Accrual

Selecting the right trial for your clinical research site is key to the success of your accrual for the trial. This eLearning course will discuss how the menu or portfolio of studies offered at a site has an important impact on accrual and how research professionals can become part of the process.

• CRC, CRN, Investigator, PR, RM

Implementing a Patient-Centered Informed Consent Process

Improve your consent process by learning how to assess a participant’s reading level, health literacy, and overall understanding of clinical trial participation and address culture, learning styles, emotional states and language. This eLearning course will provide essential tools for those directly involved in informed consent discussions.

Using Metrics to Improve Subject Recruitment and Retention

Overcome challenges in subject recruitment and retention by learning how to leverage the metrics critical to success. This eLearning course will teach site personnel assess current site performance and readiness for action, and to implement appropriate metric measurement and monitoring.

• BCO, BD, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, FA, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Introduction to Clinical Trials

Fundamental education about the role clinical research plays in advancing medical knowledge and the work conducted by clinical research professionals. This free eLearning course details how medical products are developed, how volunteer patients are protected, and key roles in the development, research, review, and approval of medical products.

• Intermediate , Senior

Site Quality Management Tools: SOPs, Metrics and Training

Master quality-related processes and procedures required to ensure trial compliance. This eLearning course is a comprehensive training program that prepares you for the next step of setting up a quality management system– essential information for site personnel involved in quality management and improvement.

• BCO, CDC, CRC, CRN, CRS, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Inspection Readiness: Best Practices for Managing Clinical Trial Inspections

Reduce your anxiety by being prepared for clinical trial inspections. This eLearning course takes you through the full cycle of a regulatory authority GCP inspection and answers key questions including: Why, when and where are regulatory inspections performed? Who can be inspected? And more.

Mastering the Event Reporting Cycle: Understanding Your Impact on Patient Safety

Efficiently identify and report safety events in your clinical trials. This eLearning course, appropriate for all clinical research professionals, guides you through the complete event reporting cycle and critical timelines, as defined in ICH E2a and E6 Guidelines.

• BCO, BD, CDC, CRC, CRN, CRS, DM, Investigator, MA, MD, MRS, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

Understanding Clinical Trial Protocols: Key Considerations for Effective Development and Feasibility Review

Expand your knowledge and skills in study protocol design and review. This e-Learning course covers the anatomy of a protocol, hypothesis development, study design, subject safety and data integrity risk considerations, protocol feasibility and protocol amendments.

Statistical Principles for Clinical Trials: Overview of ICH E9

Improve protocol interpretation and implementation by understanding trial scope, design, conduct, data analysis, and the evaluation and reporting of safety and tolerability data. This eLearning course explores the International Conference on Harmonization’s E9 guideline Statistical Principles for Clinical Trials.

• BCO, CRC, CRN, DMCTO, Executive, FA, Investigator, MCRA, PMs, RM, RTA, SSSU, Trainer

Mastering Budgeting at Your Site: Building and Negotiating Clinical Trial Budgets that Make Sense

An essential course for all clinical research professionals involved in the clinical trial agreement and/or budget process for industry-initiated trials.

Key Skills for Ensuring Quality Control through Risk-Based Decision Making

Gain confidence in making risk-based decisions and implementing actions related to quality control initiatives. This eLearning course covers key aspects related to risks in clinical trials, including: identification, analysis, planning, communication, change management and much more.

• CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Investigator, MA, MD, MRS, MSO, MW, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Statistician, Trainer

ICH Gap Analysis

Assess your and your team’s training needs quickly by conducting an ICH gap analysis. This eLearning course uses a game to challenge the learner’s knowledge and application of these important efficacy guidelines.

• Investigator, MCRA, PMs

Form FDA 1572: Get it Right the First Time

The Statement of Investigator (Form FDA 1572) doesn’t have to be complicated – let us help you get it right the first time. This eLearning course answers the questions of why, when and how to complete the FDA 1572 to make everyone’s jobs easier.

Ethics and Human Subject Protection: A Comprehensive Introduction

Explore the ethical considerations facing clinical research professionals and learn to put the rules into practice to ensure human subject safety and well-being. This eLearning course provides in-depth training on the importance of ethical conduct in clinical trials involving human subjects.

The Drug Development Process: ICH E8(R1) General Considerations for Clinical Trials

Develop a better understanding of the overall drug development process and how each study fits into the “big picture” of the development life cycle. This eLearning course puts into practice the ICH E8 guidance document General Considerations for Clinical Trials.

Building Quality Management Systems for Sites and Sponsors: Root Cause and CAPA

Implement a Quality Management System (QMS) and prevent findings related to patient safety, data quality and regulatory compliance. This eLearning course will teach you risk management strategies to avoid inaccurate trial data, regulatory non-compliance and more.

• BCO, CDC, CRC, CRN, CRS, CTMS Admin, DM, DoP, DoSA, DMCTO, DMRA, DSM, DSP, Executive, Investigator, MA, MD, MRS, MSO, MCRA, PR, Pharmacist, PMs, QCS, RS, RM, RTA, SSSU, Trainer

eResearch: Managing Clinical Trials in an Electronic Environment

Learn how to set up and manage electronic clinical research documents in compliance with U.S. and EU regulations, and current trends from both the site and sponsor perspectives. This eLearning course examines the challenges of working with electronic documents and how to overcome them.

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Home / Online GXP courses / Learning Paths / Clinical Research Associate (CRA)

Clinical Research Associate (CRA)

Skill level :

Final exam:, certificate of completion :.

CEU / CPD Accreditation:

Certification:.

Gain a recognized and traceable certificate after completing the course : 

All our certificates are unique, authentic, CPD/CEU accredited, and FDA 21 CFR PART 11 compliant. Certificates validity can be checked online through our  certificate online checker .

Description :

Discover the Clinical Research Associate Learning Path, a tailored bundle of courses expertly designed for professionals in clinical research. Guided by Dr. Patricia Kay, with her extensive background, this bundle offers deep insights into the core aspects of clinical trials.

From understanding the nuances of Good Clinical Practice to mastering Clinical Data Management, this learning path equips you with the skills and knowledge to excel as a Clinical Research Associate.

Key benefits include one-year access to updated content, a unique certification for each course, and a final certificate upon completion of the entire path.

This course is tailored for the introduction and training of both single new hires and entire teams. Whether you’re a CRA manager or a human resources specialist in charge of orienting and training anywhere from one to a hundred new CRAs, this program offers a convenient, economical, thorough, and engaging approach to training. It ensures that your new employees are being trained to the utmost industry standards, giving you confidence in their preparation.

Join now and transform your expertise in the dynamic world of clinical research.

Courses Included :

ICH-GCP Training Refresher 2024 : Good Clinical Practice for Clinical Research Professionals

Management of Clinical Trial Protocols

Clinical Data Management

Management of Clinical Study Reports

Management of The TMF and ISF

Global Pharmacovigilance Awareness

Your Expert :

This course includes:

Gxp-training benefits.

• Experts : We work with the world's top experts in GMP, GLP, GCP, GDP, regulatory affairs, QA and pharmacovigilance.
• Validated : All our courses are CPD/CEU accredited and we deliver a unique, traceable and authentic certificate to each learner.
• Self-paced : access 24/7 to the course during 12 months at your own rhythm.
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Clinical Research Associate Academy

• Level: Intermediate
• Continuing Education Units: up to 500 contact hours, 50 CEU
• Certificates: GCP, VIARES
• Duration: up to 500 contact hours, 50 CEU

THE CRA ACADEMY PROVIDES YOU WITH

Industry required competencies for a Clinical Research Associate role including

• introduction to clinical research
• understanding GCP and general regulatory requirements
• on-site trial monitoring
• remote and centralized monitoring
• monitoring oncology trials
• patient protection and informed consent
• handling of adverse events
• data management basics for clinical trials

A proven process to prepare your job application

• identify your dream job
• understand what are the requirements and how to meet them
• create a clear and concise CV
• prepare your interview
• negotiate your package

You can start your program any time after purchase and define your own pace with our online setup. This is ideal for anyone with a current employment.

ACADEMY CONTENT

Clinical research associate.

• What is clinical research
• How are clinical trials managed
• Who can participate in clinical trials
• What are the key phases and roles in clinical trials
• ICH GCP E6(R2) Certificate
• Investigator Oversight
• Background of medicines development
• Research and discovery stage & product development
• Clinical development
• Regulatory submission, Health Technology Assessment, lifecycle management
• ICH GCP and other applicable regulations
• Applicable international and national regulations
• ICH GCP E6 (R2)
• FDA Regulation
• Quality Assurance: Audits and Inspections
• Elements of a Study Protocol according to ICH GCP
• Trial Design
• Methodologies
• Ethics Committees
• Sponsor / Monitor
• Investigator
• Competent Authority
• Assessing Investigational Sites
• Training and Upgrading Investigational Sites
• Organizing the Initiation Visit
• Setting up the required documentation – Essential Documents
• Planning, Conducting, Documenting, and Reporting Monitoring Visits
• Managing Issues
• Organizing the Close-Out Visit
• Documentation
• Patient Information
• Collecting Patient Consent
• Special Patient Populations
• Types of Adverse Events
• Identifying and Reporting Serious Adverse Events
• Definition of investigational medicinal product (IMP) / study drug
• Provision of the IMP
• Drug Accountability
• Randomization, blinding and un-blinding processes
• Managing Expiry Dates
• Collecting IMP after Site Close-out
• Clinical Research Form (CRFs)
• Process of Data Collection
• Data Collection Systems
• Data validation process
• Query Process
• Data Quality Assurance

Remote & Centralized Monitoring

• Including on-site, remote, and statistical monitoring
• Regulatory guidance to remote and statistical monitoring
• Monitoring concepts in the framework of risk-based monitoring
• From concept to reality: Remote monitoring and centralized statistical monitoring
• Responsibilities
• Tools and resources
• How to handle centralized statistical monitoring
• Monitoring activity and their focus
• Documentation and follow-up
• Team interactions
• What makes a good Remote Monitor

Monitoring Oncology Trials

• Understand the characteristics of cell formation, the major causes of cancer and global impact of the disease
• Examine the impact of Oncology studies and current treatment
• Be able to discuss available treatments and objectives of treating cancer
• Examine various cancer treatments and their adverse reactions
• Explore alternative treatment options
• Identify common cancer drug and cancer combinations
• Thoroughly understand the relationship between risk and benefits of tumor therapies
• Recognize chemotherapy drug types and different principles
• Differentiate between cancer and uncontrolled tumor growths
• Recognize the six major categories of cancer classifications
• Understand components of medical terminology related to cancer
• Be able to discuss Oncology trial schematics and understand the design features.
• Be able to describe the four phases of Oncology studies.
• Understand Endpoint requirements in Oncology
• Recognize common clinical assessments related to oncology trials
• Gain proficiency in reviewing clinical reports
• Identify disease history and common Inclusion/Exclusion criterion
• Define each line of therapy and understand the timing of each line
• Understand dosing design in oncology studies
• Recognize most common Adverse Events and be able to discuss clinical events related to oncology studies
• Recognize common toxicities and understand the DLT process
• Be able to discuss recruitment challenges in Oncology studies
• Describe the screening and enrollment process
• Understand the role of the medical monitor and various key members during screening process
• Clinical Reports and Source
• Distinguish between RECIST 1.0 and RECIST 1.1
• Utilize appropriate oncology disease progression algorithms
• Understand disease progression
• Prepare for challenges with site structure and Delegation of Responsibility at oncology sites 
• Describe key site staff and associated roles
• Discuss the key function of site staff
• Learn Sponsor/CRO expectations of Oncology Monitors
• Understand the stress and pressures of monitoring oncology studies
• Learn time saving techniques while monitoring

Application support program

included with one-time payment plan

• Setting clear goals and expectations is the crucial first step when it comes to your job search.
• Understand WHAT are the required skills of your dream job and how to acquire them 
• you will address THE most important piece to get your dream job
• As often, it’s more about preparation and practice than any other “miracle tip”. There is no secret – however, there is a good way to prepare correctly for any interview (a method), and this method works well.
• Negotiate and Get What You Truly Deserve.

3 VIARES CERTIFICATES

Upon enrollment you will receive your first certification “Confirmation of Enrollment”. After successful completion of the program and your exams, you get 3 (C linical Research Associate, Remote & Centralized Monitoring, Oncology CRA)   personal certificates including:

• course title
• contact hours
• continuing education units (CEU)
• your overall course score
• date of completion
• personal certificate verification code

We also show you how to best share your certificate on LinkedIn and other social media platforms.

Obtaining your certificates can provide several potential benefits, including:

• Professional recognition: A Clinical Research certification demonstrates to employers and colleagues that you have the knowledge and skills necessary to excel in your role as a clinical research professional.
• Competitive edge: In a competitive job market, having a Clinical Research certification can set you apart from other candidates and increase your chances of being hired or promoted.
• Career advancement: With a Clinical Research certification, you may be eligible for higher-paying and more advanced roles in the field.
• Increased knowledge and skills: Pursuing a Clinical Research certification can help you gain a deeper understanding of clinical research methods, regulations, and ethical considerations, which can help you perform your job more effectively.

Overall, obtaining a Clinical Research certification can be a worthwhile investment for those who are committed to their career in clinical research and interested in advancing their knowledge and skills.

Your expert instructors

BARTEK JAROSZ

Gabi Disselhoff

GAVIN CHAIT

Joanna Wilinska Mackowiak

Andreas Beust

PATRICIA HOLLIS

Hear from our graduates.

The VIARES Talent Program was indeed an amazing opportunity for achieving more in-depth knowledge regarding Clinical Trials and a start-up to my future career advancement in Clinical Research field. The training is quite extensive, meticulous and

vibrant with seasoned and supportive instructors. I strongly recommend the VIARES Talent Program.

It was a pleasure taking part in the VIARES Clinical Research Talent Program. The program was well organized, excellently structured, and the topics were taught by experts in the field. This intensive course covered all essential topics needed

by professionals who have great interest in clinical research to start a career in the industry and carry out trial-related tasks. Thank you, Viares!

Customer Reviews

Alot of content relevant to my area of work.

The course structure is very simple to follow and above all the topics are taught by experts in the field.

Awesome Self explanatory course. User friendly and easy to navigate and work it out. A love the fact that it keeps tabs with previous topic location.

It is well explained and easy to understand , It opened my eyes to the highly new research world.

reviews curated by judge.me

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Clinical Research Career Accelerator

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18 Years experience

Bartek has 18 years experience in clinical research business, mostly spent at largest global Contract Research Organizations. At Quintiles he was responsible for pioneer development of clinical start-up and regional contract departments. He served as executive member of clinical start-up leadership team at INC Research, acting as global head of site contract division. His most recent experience includes support for pharmaceutical organizations in various project specific roles. Bartek enables biopharma to get their sites up and running faster. He is author of several training programs about site contract related matters and successfully delivered to hundreds of individuals worldwide.

38 years in pharmaceutical development

Gabriele is currently the Managing Director of CRQS (Creative Regulatory & Quality Solutions), specializing in Strategic Regulatory Affairs, Quality Management, Organizational Development and Change Management. She has 38 years of experience under her belt in pharmaceutical development, with 29 years in pharmaceutical industry (Merck KGaA, Abbott) and 9 years consulting. She has extensive industry experience in regulatory affairs, clinical research and clinical quality assurance, and a thorough knowledge of document management and electronic submissions.

Data Scientist at Whythawk

Gavin Chait is a Data Scientist at Whythawk, which specializes in integrated open data consulting, and training for open knowledge, freedom of information, and economic development projects. He spent more than a decade in economic and development initiatives in South Africa. He was a commercial director at the Open Knowledge Foundation, and led the implementation of numerous open data projects around the world. Gavin has twenty years of experience in teaching at all academic levels, and is a passionate advocate for knowledge development through open access to data and freedom of information.

in the industry for 21 years

Patricia has been in the clinical research industry for over 20 years. She began her career as a clinical research coordinator at the Medical College of Virginia where she coordinated pharmaceutical and PI initiated trials. She has been a Clinical Research Associate for 16 years and has had the opportunity to serve as a Lead CRA, Clinical Trial Manager, Auditor, Mentor, and Clinical Research Instructor. She has worked in all phases of research and is experienced in numerous therapeutic areas, including Oncology, Endocrinology, CNS, Immunology, Cardiology, Nephrology and Device. Currently, she is a contract CRA through her company, The Hollis Group, LLC, which she owns with her husband and serves as a consultant at local research sites. Patricia completed a Bachelor of Science degree at Virginia Commonwealth University, MBA at Texas Woman’s University and has had specialized oncology training from the Oncology of Nursing Society.

Request Course outline

Explore our pricing plans, 12 payments.

• One year access to your training courses
• Personalized certificate upon completion
• VIARES exam – 2 attempts included
• All online-training course material
• Online access to our learning management system
• One year access to your training courses​
• VIARES exam – 2 attempts included​
• Including the VIAES CAREER ACCELERATOR
• Plan ends automatically after 12 payments
• No training course handouts for offline learning
• No unlimited access
• All benefits from the montly payment plan
• Life-time access to your purchased course
• Training course handouts included
• Life-time support from the VIARES tutors
• And much more...

CLINICAL RESEARCH ASSOCIATE (CRA) BEGINNER

As a CRA you'll be responsible for the managerial aspects of various clinical trials at every stage of the process.

Very good course! The group discussions and the anecdotes/industry insight provided was extremely helpful. Talking to the tutor and other delegates with experience and insight into the role of a CRA was invaluable.

Jacob Lawman, Clinical Data Management & Monitoring Associate Research Organisation (KC) Ltd

GET TRAINED WHEREVER YOUR LOCATION

Online instructor-led course.

Mon 13 th – 29 th May 2024

Mon 09 th – 25 th Sept 2024

Mon 11 th – 27 th Nov 2024

Mon 17 th Feb – 05 th Mar 2025

Mon 12 th – 28 th May 2025

Mon 08 th – 24 th Sept 2025

Face to face

Mon 22 nd – 24 th Apr 2024

Mon 15 th – 17 th July 2024

Mon 28 th – 30 th Oct 2024

Mon 20 th – 22 nd Jan 2025

Mon 14 th – 16 th April 2025

Mon 14 th – 16 th July 2025

All our courses are accredited by CPD, the UK's largest independent accreditation service, and delivered by highly experienced clinical professionals.

Receive your industry recognised certification at the end of the course and your learners reference manual!

What prior knowledge is needed.

Most CRA positions require as a minimum a BSc in:

• Biological/life sciences
• Related medical field or a nursing qualification

However, in some cases, CRAs have entered the profession without a graduate degree but have the relevant expertise. The most important thing is having the right skills for the job.

Read our blog: Could A Clinical Research Associate (CRA) Position Be The Role For You?

COURSE DESCRIPTION

If you are looking to enter the field of clinical research, this CPD-accredited 3-day course is for you. It will provide you with a comprehensive insight into an entry-level Clinical Research Associate (CRA) role.

This fundamental "how-to" and "why" course, focuses on current practice. You will learn about the CRA's role and responsibilities in the context of the regulations and rules that govern clinical trials. You will look at a day in a CRA's life to gain insight into the profession. Alongside this, you will review mock-up sample protocols and study documents to reinforce your learning.

For information on the intermediate or advanced level CRA course, please send us an email at [email protected] or book a consultation with us.

What will be covered in this course?

This module will look at:

• The primary duties of a CRA
• The specific responsibilities in accordance with ICH-GCP
• SOP and regulations for before, during and after a clinical trial
• Essential documents — Preparation, collation and QC
• Ethics and regulatory submissions and approvals of the clinical trial application
• Study start-up activities — site identification and selection, QC for IP release
• Site activation — SIV, ISF review and drug supply review
• Monitoring and site management
• Study site closeout activities

You will also be guided through some real-life practical training that you will experience on the job.

• Scenario based training
• Group workshops
• Review a Monitoring Plan for a clinical trial
• First-hand review and practical use of drug accountability logs, and returned investigational product kits
• Video: A Day in the Life of a Clinical Research Associate

Excellent course, excellent tutor, really knew her stuff. A lot of material covered. Gained huge knowledge of the role of a CRA.

Angeline Nwoko, CTA, London

Who is the course designed for?

If you are a clinical trial administrator who has just been promoted to a CRA level I or have limited experience as a CRA, this modular training is specifically designed for you.

This is a good starter course that will equip you with the skills to conduct clinical trial initiation and/or monitoring and basic site management at the investigational site.

FREE CONSULTATION WITH CGX HEAD TRAINER

Book a free consultation with our Head Trainer to find 
out more about our courses and the best fit for your 
future career in clinical research.

MEET YOUR EXPERT TRAINERS

With a BSc in Chemistry, PhD in Organic Chemistry and a Postdoctoral Research Fellowship at the Institute of Biotechnology at Cambridge University, Dr Lia Hunter's career has spanned 30 years in clinical research. Founder and Director of both CGX Training and Clinnovate Ltd, Dr Hunter has worked for and with world-renowned pharmaceutical organisations, including Pfizer, Biogen, Takeda and AbbVie.

Donna-Marie Donalds’ career has spanned more than 20 years. Starting as a CRA for the Thrombosis Research Institute in 2001, she has since worked with the likes of Johnson & Johnson, Covance and Sanofi-Aventis. She is currently the Managing Director of QC Monitoring Solutions while freelancing as a clinical research consultant. Donna-Marie is also Head of Training and the innovative course creator at CGX Training.

IT'S TIME TO INVEST IN YOURSELF

Stepping into the clinical research industry can feel overwhelming. if you don't know where to start...start here.

If you’re a clinical trial administrator who has just been promoted to a clinical research Associate level I or currently a CRA that wants to ensure you’re performing to GOLD STANDARD so you can progress in your career, this is the course for you.

The CRA course has been specifically designed with live mock scenarios to arm you with the on-the-job skills you need. Plus, you'll also be carefully guided through the job application process, with insider tips on how to create a standout CV and nail that interview.

Want to see where one of our CRA trainees is now?

Read our blog: Graduate Profile — Jack Moody — CRA Beginners Course & CPM Beginners Course

think your organisation could benefit from tEam training?

Visit our Corporate Training page for more information

• Live In-Person Conferences

Clinical Research Never Stops Advancing, Neither Should You

SOCRA offers a robust portfolio of live in-person conferences, workshops, and courses to keep you at the forefront of the industry and support your continuing educational goals. See below for a full list of live programs, or visit the event calendar .

Decentralized Clinical Trials

 In this workshop, you'll gain a solid understanding of the fundamental considerations for DCTs and learn practical approaches to designing, administration, and implementation.

CCRP Preparation and GCP Review Course

Aids participants in preparing for the CCRP certification exam through review of FDA and ICH Good Clinical Practice (GCP) guidelines.

Project/Program Management

Presents project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

Site Coordinator / Manager & GCP Workshop

This workshop, for site coordinators, research associates, and study nurses, will review the responsibilities at the clinical research site.

Quality Management Conference

 This conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

FDA Regulatory Requirements, Compliance, & GCP Conference

Shares information regarding clinical research regulations and GCP guidelines and discusses methods to aid the research professional in their practice.

Pediatric Clinical Trials Conference

Covers the regulatory, financial, and ethical components of conducting clinical trials in the pediatric population.

Device Research & Regulatory Conference

Discusses current issues relating to compliance, development, and clinical investigation for Device Research.

Oncology Clinical Trials Conference

Assists Research Professionals in improving their skills and their understanding of the responsibilities of conducting oncology clinical research.

Human Research Protections

Aids participants in understanding the legal, ethical and practical considerations related to human subjects research.

Finance & Productivity Workshop

Assist in improving skills and understanding of the practical financial and business tasks related to clinical research.

Monitoring & GCP Workshop

Reviews GCP and clinical research monitoring best practices for site monitors, managers or auditors, in an interactive format. 

Clinical Research Nursing

Presents the essential functions of the clinical research nurse with consideration of the recently released ANA Scope and Standards of practice for Clinical Research Nursing.

Canadian Regulatory Conference

Assists clinical research professionals in improving their skills and understanding of the responsibilities of conducting clinical research in Canada.

Advanced Concepts for Clinical Investigators and Key Research Staff

Presents GCP, finance, budgeting and legal responsibilities of the clinical investigative site.

Emergency Clinical Research Symposium

Assists Research Professionals in improving their skills and their understanding of the responsibilities of conducting clinical research in the emergency setting.

Quality Improvement through Standard Operating Procedures (SOPs)

Discusses fundamental concepts and current issues in the development and implementation of an effective SOP program for clinical research.

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OFFICE OF CLINICAL RESEARCH EDUCATION AND COLLABORATION OUTREACH

Clinical research education.

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One of NIH's goals is "to develop, maintain, and renew scientific, human, and physical resources that will ensure the Nation's capability to prevent disease." Training and education are the means to provide these capabilities. The Office of Clinical Research Education and Collaboration Outreach has the responsibility for courses which provide clinical research training for the spectrum of investigators and others involved in clinical research.

• Introduction to the Principles and Practice of Clinical Research
• Principles of Clinical Pharmacology
• Ethical and Regulatory Aspects of Clinical Research
• NIH Summer Course in Clinical and Translational Research
• NIH-Duke Master's Program
• Sabbatical in Clinical Research Management

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Clinical Research Associate is considered to be the most sought out jobs in the clinical research industry. The research industry has struggled to find quality trained CRA’s and our goal is to fill this gap through intensive training courses and hands on courses.

Clinical Research Associate (CRA)

• CRA – Level I –    3 months hands on training.
• CRA – Level II –   6 months hands on training – Most Popular
• CRA – Level III –  9 months hands on training
• CRA – Level IV – 12 months hands on training

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What people are saying.

According to other learners, here's what you need to know

academic writing in 6 reviews

Although I have attended many online and life courses on scientific and academic writing there is always something new to learn and master.

I kind of wish it had more examples of language to use in academic writing, contrasting good and bad examples.Some of the quiz questions and final exam questions need some proofreading.

There are a number of useful guides for new researchers to learn how to structure, phrase, and approach academic writing.

Some of the material is overly subjective (giving rules for academic writing that are not necessarily applicable).

Finally, the course relies too heavily on academic writing for the hard sciences, rather than taking a broader approach, so some students may wish to keep this in mind when watching, as some advice may not be applicable to their own discipline.Overall, a recommended course for ESL academics, but could do with some improvement.

It was useful to know so many nuances 'bout how the academic writing works.Completely updated my knowledge.

Discovering many new things about academic writing articles.

research paper in 3 reviews

During this course, I learned so many tips for writing a good research paper in English.

It helped me crystallize what I didn't understand about writing a research paper before.

prof. e. bazanova in one review

the lecturer need to develop his way of communications with students First, Prof. E. Bazanova started with very basics.

At the end of this course, Prof. E. Bazanova was given a great idea how to design a scientific paper.

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Clinical Research Associate (Client Onsite) - CRA - Moscow

🔍 moscow, russia, russia.

• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Effective independent clinical monitoring skills ;
• Excellent understanding and demonstrated application of GCPs and applicable SOPs
• Management of regulatory and / or IEC questions
• Development and preparation of the local informed consent form
• Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
• Management of the delivery of study supplies
• Strong customer focus
• Effective interpersonal skills
• Strong attention to detail
• Effective organizational and time management skills
• Proven flexibility and adaptability
• Ability to work in a team or independently as required
• Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills
• Good presentation skills  
• Requisition ID: 126817