Certificate Program for Clinical Research Coordinator (CRC)

This online & self-paced certificate course will provide you a comprehensive training required to execute the job functions of a clinical research coordinator (CRC) in compliance with ICH-GCP & applicable regulatory guidelines.

  4.5 (1024 Ratings) 

Enroll Now
Certificate Program for Clinical Research Coordinator

Curriculum

Learning Objectives

Testimonials

FAQs

About the Course

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

CPCRC is an online & self-paced certificate program which will provide you a comprehensive training on scientific, financial, practical, ethical and technical concepts of clinical trials and the entire job functions of a clinical research coordinator during a trial. This 10 weeks training course covers an in-depth training for the role of Clinical Research Coordinator (CRC) in 25 modules covering 300+ topics. Each module is well explained in detail with the help of illustrations, templates, examples, and flowcharts.

Who Should Enroll?

This course is specially designed for:

  • Health-science candidates (Pharmacy, Life-Science, Medicine, AYUSH, Dental, Nursing, Physiotherapy, Ph.D. etc.) who are looking to gain knowledge & start their career as Clinical Research Coordinator
  • Fresher and experienced clinical research personnel (CRCs, CRAs, Project Managers, Research Nurse etc.)

Rs.11200 Rs.14000 20% Off

20% Fee Discount until Nov 15th
Last Date: 30th November 2024
Learning: Online & Self-paced
Duration: 6 Months
Fee: INR 11200 / USD 175
Assessment: Online Single Exam
Course Login Access: Immediate
Content Access: Lifetime
Efforts: 80 Hours Approx.
Includes: Certificate of Completion
Enroll Now

Benefits After Enrollment

JOB ORIENTED CURRICULUM

Our course modules covers all the elements required to impart skills & knowledge to get a relevant job in the industry.

GLOBALLY VALID CERTIFICATE

Our course modules are based on ICH-GCP and applicable regulatory guidelines which are valid globally. So, The certificate is acceptable across the industry.

PLACEMENT ASSISTANCE

Upon course completion we help you with placements through our referrals and industry experts for the relevant job positions.

RESUME & INTERVIEW

Along with placements, we also assist you to prepare your resume as per the industry standards along with interview preparation.

Enroll & Get A Free Beautifully Designed Resume

You Have Less Than 6 Seconds to Impress the Employer.

When you enroll in a course, we transform your dull-looking CV into a “beautiful & professional CV” to make it stand out from the rest for free of cost.

We help our course participants to redesign their CV/ resume as per industry standards. This amplifies their chance to get selected for the relevant job positions.

Learn How

Course Curriculum

I

Module 1: Introduction to Clinical Research

 
I

Module 2: Ethics and Guidelines in Clinical Research

 
I

Module 3: Roles & Responsibilities of Trial Personnel

 
I

Module 4: Introduction to Clinical Research Coordinator

 
I

Module 5: Essential Clinical Trial Documents

 
I

Module 6: Investigator Site Feasibility

 
I

Module 7: Site Budget, Payment Schedule & Negotiation

 
I

Module 8: Clinical Trial Agreement (CTA) & Negotiation

 
I

Module 9: Investigator Training Meeting

 
I

Module 10: Institutional Review Board (IRB) Submission

 
I

Module 11: Site Initiation Visit (SIV)

 
I

Module 12: Investigator Site File (ISF)

 
I

Module 13: Clinical Trial Registration

 
I

Module 14: Procurement

 
I

Module 15: Subject Screening, ICD, Recruitment & Safety

 
I

Module 16: Source Documentation

 
I

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

 
I

Module 18: Safety Reporting & Management

 
I

Module 19: Monitoring Visit

 
I

Module 20: Audit & Inspection

 
I

Module 21: Investigational Product (IP) Management

 
I

Module 22: Financial Management

 
I

Module 23: Communication, Coordination & Compliance

 
I

Module 24: Site Closeout Visit

 
I

Module 25: Site Closeout Activities

 

How This Works?

Upon enrollment, the course participant will get the course login details before the start of batch via email.

Upon receipt of course login details, the participant can log in to take the course modules anytime and from any device.

After reading all the course modules, the course participant is required to attempt and submit an online exam.  

Upon evaluation of exam, the certificate of completion will be issued to all the successful participants of the batch.

Learning Objectives

At the end of the course, you should be able to:

Z

Learn the concepts of clinical research, GCP & applicable guidelines

 
Z

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

 
Z

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

 
Z

Develop skills to handle during trial responsibilities (ICD process, IP Management, Safety Reporting, source documentation, CRF entry, audits, monitoring visit etc.)

 
Z

Learn the site-close out activities

 
Z

Effectively manage the quality of clinical trial activities.

 

Participant’s Feedback

Average Rating

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

Clinical Research Coordinator

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

Trial Coordinator

A must take course for all the clinical research coordinators but only if you are not certified as CRC.
Abdul Gaffar

Clinical Research 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

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

Scientist

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

Project and Team Manager

Top FAQs

Is it 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 exam, and certification of completion.

Do I have to take the course on specific timings?

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

Can I complete the course early also?

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

I am a very 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@physislearningacademy.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 second and final chance to attempt the exam.

How can I pay the fee?

To enroll and pay the course fee, follow the link STEPS TO ENROLL

You Might be Interest In 

Have A Query? Contact Us.

Share This