Certificate Program for Clinical Research Coordinator (CRC)

Become A Certified Clinical Research Coordinator with this online and self-paced course. The Clinical Research Coordinator Certification program will train you to efficiently manage & coordinate the day-to-day trial activities of a Trial Coordinator at a study site in compliance with applicable regulatory guidelines.

  4.6 (750+ Ratings)  3780+ participants enrolled

About This Course

The clinical Research Coordinator (CRC)/ Clinical Trial Coordinator is trial personnel responsible for the coordination, management, and ethical conduct of clinical trial activities at the trial site and under the guidance of the study investigator. A CRC plays a vital role in clinical trials and acts as a principal link of communication between the principal investigator, sponsor, and institutional review board (IRB).

If you are looking to start your career as a CRC or you are already a research coordinator without any formal training, the CRC certification course will certify and train you to develop the required knowledge and skills of a Clinical Research Coordinator.

The 25 in-depth course modules of this course will train you to efficiently manage & coordinate the day-to-day trial activities of a Clinical Research Coordinator at a study site in compliance with ICH-GCP and applicable regulatory guidelines. Each training module is explained in detail with the help of illustrations, templates, examples, and flowcharts.

Who Should Enroll?

The course can be attended by:

Any researcher and healthcare professional (fresher/working) who is looking to take the training & start their career for the job position of a Clinical Research Coordinator (CRC)

Fresher and experienced clinical trial personnel

Nurses interested to develop a career in clinical research

Other specialists from Medical Affairs, Pharmacovigilance, Pharmaceutical Development Scientists, Translational Medicine, Regulatory Affairs etc.

$256 $320  20% Off

Course Highlights

20% Fee Discount until May 20

Last Date: May 25, 2024

Online and Self-paced Learning

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Single Online Exam

10-weeks Duration
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Approx. 40 Hours of Effort

Global Acceptance

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Lifetime Access to Content
Immediate Access
Includes Certificate of Completion

Course Curriculum

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Module 1: Introduction to Clinical Research

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Module 2: Ethics and Guidelines in Clinical Research

 
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Module 3: Roles & Responsibilities of Trial Personnel

 
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Module 4: Introduction to Clinical Research Coordinator

 
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Module 5: Essential Clinical Trial Documents

 
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Module 6: Investigator Site Feasibility

 
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Module 7: Site Budget, Payment Schedule & Negotiation

 
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Module 8: Clinical Trial Agreement (CTA) & Negotiation

 
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Module 9: Investigator Training Meeting

 
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Module 10: Institutional Review Board (IRB) Submission

 
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Module 11: Site Initiation Visit (SIV)

 
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Module 12: Investigator Site File (ISF)

 
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Module 13: Clinical Trial Registration

 
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Module 14: Procurement

 
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Module 15: Subject Screening, ICD, Recruitment & Safety

 
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Module 16: Source Documentation

 
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Module 17: Case Report Form (CRF) & Data Entry

 
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Module 18: Safety Reporting & Management

 
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Module 19: Monitoring Visit

 
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Module 20: Audit & Inspection

 
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Module 21: Investigational Product (IP) Management

 
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Module 22: Financial Management

 
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Module 23: Communication, Coordination & Compliance

 
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Module 24: Site Closeout Visit

 
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Module 25: Site Closeout Activities

 
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Assessment Through Online Exam

How Does This work?

You will get the course access details within 48 hours of enrollment.

After that, you can log in to take the course modules at your pace and timings from any device.

After finishing all the course modules, you have to attempt and submit an online exam. The exam is also self-paced. 

After reviewing your exam, the certificate of completion will be issued to all the successful participants of the batch.

Learning Objectives

This course will help you to learn about

Basic concepts of Clinical Trials, Good Clinical Practice (GCP) and applicable regulatory guidelines

Develop the required skills & knowledge to coordinate and manage a clinical trial site

Develop skills to handle pre-trial responsibilities (trial training, negotiation, site feasibility, agreement etc.)

Develop skills to handle during trial responsibilities (ICD Process, IP Management, Safety Reporting, Source Documentation, CRF entry, Audits, Monitoring visit etc.)

Site-close out activities

Effectively manage the quality of clinical trial activities.

Learners From Top Schools and Companies

To date, learners from 65+ countries and 160+ prestigious global schools and organizations are enrolled in this course.

Testimonials

Average Rating

I was not expecting to cover this much information in this course. But the instructor has covered detailed information for Clinical Research Coordinators. Well Done.

Lynn Hoffmann

Clinical Research Coordinator

A must-take course for all the research coordinators and aspirants.

Abdul Gaffar

Clinical Research Coordinator

Overall the course was very interesting and the information was presented well.

Sabrina Michael

Scientist

The course was a bit lengthy but thank you for granting the extension to finish it.

Alexandra Lyon

Trial Coordinator

I took this course along with colleagues to be a certified clinical research coordinator. I am thankful to the instructor for resolving all of my queries.

Rabeeah

Research Assistant

I have already taken a prior online course as a clinical research coordinator. Few topics were new. I liked the exam and evaluation part.

Katie Green

Project and Team Manager

Top FAQs

Is this the entire course fee?

Yes, the fee mentioned above is the entire course fee and there is no additional fee attached to this course. The fee covers the cost of course modules, online exams and certification of completion.

Do I have to take the course at specific timings?

There is no need to take the course module at particular timings. The course is self-paced and you can take the modules anytime.

Can I complete the course early also?

Yes, you can. To do so, you have to attempt and submit the online exam for evaluation.

I am busy with my professional work/ studies. What if I don’t complete the course on time?

In this case, you can extend the timelines to complete the course. You can do so by dropping a request email in advance with your registered email id at info@physisglobalacademy.com

What if I don’t clear the exam?

Though the course modules are self-explanatory and you can comfortably clear the exam if you go through all the course modules. But in case you are unable to clear it in your first attempt then you will get a second (final chance) to attempt the exam.

How can I pay the fee?

To pay the course fee, follow the link STEPS TO ENROLL or you transfer the applicable course fee directly through your PayPal account to our PayPal account at info@physisglobalacademy.com

Interested in group enrollment?

Get up to a 50% discount when you sign up for our plans customized for individuals and companies.

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