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.
$240 $320 25% Off
Course Highlights
25% Early Bird Off until April 7
Last Date: April 25, 2025
Online and Self-paced Learning
Single Online Exam
Approx. 40 Hours of Effort
Global Acceptance
Course Curriculum
Module 1: Introduction to Clinical Research
Module 2: Ethics and Guidelines in Clinical Research
Module 3: Roles & Responsibilities of Trial Personnel
Module 4: Introduction to Clinical Research Coordinator
Module 5: Essential Clinical Trial Documents
Module 6: Investigator Site Feasibility
Module 7: Site Budget, Payment Schedule & Negotiation
Module 8: Clinical Trial Agreement (CTA) & Negotiation
Module 9: Investigator Training Meeting
Module 10: Institutional Review Board (IRB) Submission
Module 11: Site Initiation Visit (SIV)
Module 12: Investigator Site File (ISF)
Module 13: Clinical Trial Registration
Module 14: Procurement
Module 15: Subject Screening, ICD, Recruitment & Safety
Module 16: Source Documentation
Module 17: Case Report Form (CRF) & Data Entry
Module 18: Safety Reporting & Management
Module 19: Monitoring Visit
Module 20: Audit & Inspection
Module 21: Investigational Product (IP) Management
Module 22: Financial Management
Module 23: Communication, Coordination & Compliance
Module 24: Site Closeout Visit
Module 25: Site Closeout Activities
Assessment Through Online Exam
How Does This work?
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.
A must-take course for all the research coordinators and aspirants.
Overall the course was very interesting and the information was presented well.
The course was a bit lengthy but thank you for granting the extension to finish it.
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.
I have already taken a prior online course as a clinical research coordinator. Few topics were new. I liked the exam and evaluation part.
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
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