Professional Certificate in Clinical Research (PCCR)

Advance your career with the online clinical research certificate. This clinical research certification program will provide you training and skills on clinical trial regulatory guidelines, roles, and responsibilities of clinical research stakeholders and personnel, clinical trial study processes, etc. This course will also help you to prepare for global entry-level job positions in the clinical research industry.

4.7 Average Rating (4800+ Course Participants)

$120 $150

20% Fee Discount until March 31

March 2024 Batch

Last Date of Application: March 31, 2024

Online & Self-Paced

40-50 Hrs. of Efforts Required

Course Overview

Professional Certificate in Clinical Research (PCCR) program enables learners to take in-depth knowledge of ICH-GCP and applicable regulatory guidelines, clinical trial study processes, roles, and responsibilities of various stakeholders, ERB, Informed Consent Document Process, SAE Reporting procedures, Clinical Trial Source Documentation, Terminologies, etc.  Check the complete Course Curriculum.

The clinical research training course will prepare the aspirants and working professionals to excel career in Clinical Trial Operations as Clinical Research Coordinator (CRC), Clinical Trial Assistant, Clinical Research Associate (CRA), or Clinical Trial Investigator.

Course Features

A

Course Fee: $120 (20% Discount)

A

Batch: March 2024

A

Last Date: March 31, 2024

A

Course Duration: 12 weeks

A

Certificate Validity: Global

A

Timings: Self-Paced

A

Mode of Learning: Online

A

Exam: Single, Online

A

Efforts: Approx 40 to 50 Hours

A

Content Access: Lifetime

A

Language: English

A

Includes: Exam Fee and Certificate of Completion

Course Curriculum

Clinical Research course syllabus covers the following training modules:

I

Module 1: Introduction to Clinical Research

I

Module 2: Evolution of Ethical Research principals, Regulations and Guidelines

I

Module 3: Essential Clinical Trial Documents

I

Module 4: Clinical Study Process

I

Module 5: Ethics Review Board (ERB)

I

Module 6: Roles and Responsibilities of Investigator

I

Module 7: Roles and Responsibilities of Sponsor

I

Module 8: Roles and Responsibilities of CR Personnel (Clinical Trial Coordinator, Clinical Trial Associate, ERB, Biostatistician)

I

Module 9: Informed Consent Process

I

Module 10: Serious Adverse Event (SAE)

I

Module 11: Maintenance of Source Document

I

Module 12: IND/ NDA/ ANDA/ AADA

I

Clinical Trials Terminology

l

Assessment through Self-paced Online Exam

Learner’s Profile

Online clinical research course caters to global health science working professionals, masters, and graduates from international medical schools and universities, CROs, and healthcare companies. Participants from 60+ countries are part of this clinical trial program.

Schools, Universities and Companies
Alexion Pharmaceuticals, Inc.
Tecnológico de Monterrey
The University of North Carolina at Chapel Hill
The Children’s Hospital of Philadelphia
Seattle Pacific University, USA
University of Yaoundé
Region-wise Distribution of Course Participants
Chart by Visualizer
Testimonials

Happy Learners

Nadia Castioni

Entry-level CRA, Italy

I really appreciated this course. It has been very useful to me as it allowed me to get sufficient knowledge of the field to get a job as an entry-level CRA.

Kwizera Marie Ange

MD, Infectieuse Deseases Scientist, Russia

I’m personally satisfied with this clinical research certificate course. It is a very important course that a high number of people ignore.

Homero Castano

Clinical Research Coordinator, US

Maximum coverage by the trainers in creating the course curriculum and content.

R Rasheed

Clinical Trial Coordinator, Egypt

Had a wonderful experience after enrolling in Clinical Research with Pharmacovigilance combined certificate. Special thanks to the trainer for extending my timelines to complete the course examination.

Dr James Williamson

Clinical Trial Investigator, US

PCCR course has everything in the syllabus to know the basics of a clinical trial.

Arabjeet Ghosh

Research Coordinator, India

It was to the point and applicable in my current profile. Shall surely recommend to my team members.

Course Eligibility

  • Clinical Research Professionals
  • Aspirants (graduates, masters, PhD and working professionals) from health science background: Pharmacy, Medicine, Dental, Nursing, Public Health, Life-Science, Biotechnology, Physiotherapist, Traditional/ Alternative Medicine etc.

Enrollment Process

The enrollment process consists of 3 simple steps to enroll in the course.

STEP 1: ADD TO CART

Click Enroll Now Button, Click Add to Cart Button, and Click Proceed to the checkout button.

Z

STEP 2: FILL THE DETAILS

Fill your personal and billing details on the checkout page, Check T&C Box and Click Pay Now Button

STEP 3: PAY THE FEE

Pay the course fee securely via PayPal with your Card or Net Banking & get immediate access to the course.

To know step by step process visit the Page HOW TO ENROLL

Course Benefits

  • 12 online self-paced learning modules (approx. 40 hrs. of learning).
  • A self-paced online exam for your assessment.
  • Certificate of Completion and a Performance Sheet on successfully completing the course.
  • Opportunity to explore a career in Clinical Research Operations as Research Coordinator, Clinical Research Nurse, Research Assistant etc.
Certificate in Clinical Research Sample

Interested to enroll in 2 or more courses?

Save more with our Course Plans made for individuals and teams.

Top FAQs

When will I get access to the course after paying the fee?

It generally takes up to 48 hours to email you the course login credentials.

Can I complete the course earlier than 12 weeks?

Yes, you can.

How will the course modules be delivered to me?

We will email you the log in information. You can access our learning portal with the provided details. 

I am a busy working professional; can I take this course?

Yes, more than 80% of course participants are working. The course modules are completely self-paced. So, you can finish the course at your own pace and time.

I am a student at present; can I take this course along with my studies?

Yes, you can take this course along with your regular studies.

Is there any specific time to take the course modules?

No, the modules are self-paced. You can learn the module as per your convenience.

How do you conduct the exam?

Once you are through with the course modules and want to take the examination, you just need to drop us an email to get access to the exam.

A request to take the online exam can be forwarded at any point in time.

When will I receive the certificate and performance sheet?

We generally take up to 14 working days to evaluate you and issue a Certificate of Completion with Performance Sheet after submission of your exam.

How will you send me the certificate of completion?

A print-ready Certificate of Completion will be issued through email upon successful completion.

Can I pay the fee in installments?

Yes, you can pay the fee in a maximum of two installments. To pay the fee in installments, you need to contact us at admin@dnasysacademy.com

You can also check our FAQ page for further queries.

More Courses

CRC Certificate Training

Certification Training for Clinical Research Coordinator (CRC)

Pharmacovigilance Course

Professional Certificate in Pharmacovigilance (PCPhV)

Professional_Certificate_in_Clinical_Research

Professional Certificate in Clinical Data Management (CDM)

CRA Certification

Certification Training for Clinical Research Associate (CRA)

Send Us Your Query

Email us at admin@dnasysacademy.com or fill out the below form.