Dual Certification in Clinical Research & Medical Writing (DCCRMW)

This self-paced dual certificate course will provide you a comprehensive training on clinical trial processes and the steps to design essential trial documents. This course will also train you for the entry-level job positions in clinical research & medical writing (Clinical Research Coordinator, Trial Assistant, Medical Writer etc.)

  4.5 (196 Ratings)

About the Course

With 250000+ clinical trials already registered at clinicaltrials.gov portal, the present worth of global clinical research industry is estimated to be more than $40B. ICH-GCP and regulatory guidelines provide a framework of principles which aims to ensure the safety of study subjects along with integrity and validity of data produced during trials.

As per the Center Watch market research analysis conducted in 2008, the medical writing industry has grown at the rate of 15% each year for the last five years to staggering USD 700 million.

Dual Certification in Clinical Research and Medical Writing (DCCRMW) will provide you a comprehensive training on scientific, practical, ethical and technical concepts of the clinical trial & strategies required to design clinical trial documents. This 6 months course covers the essential knowledge in 22 course modules. Each module is well explained in detail with the help of illustrations, 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 in clinical research as Clinical Research Coordinator or medical writer.
  • Fresher and experienced Clinical Research personnel.

Rs.11200 16000 30% Off

30% Fee Discount until 25th Nov
Batch Starts 30th Nov'2018
Learning: Distance & Online
Duration: 6 Months
Efforts: 100 Hours Approx.
Assessment: Single Exam
Includes: Certificate of Completion
Course Access: Lifetime

Course Curriculum

Clinical Research

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Module 1: Introduction to Clinical Research

 

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Module 2: Evolution of Ethics, Regulations & ICH-GCP

 

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Module 3: Roles and Responsibilities of CR Personnel

 

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Module 4: Clinical Study Process

 

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Module 5: Institutional Review Board (IRB)

 

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Module 6: Informed Consent Process

 

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Module 7: Study Subject Recruitment & Retention

 

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Module 8: Safety Reporting & Adverse Event Management

 

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Module 9: Research Protocol

 

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Module 10: Essential Research Documents

 

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Module 11: Maintenance of Source Documents

 

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Module 12: Site Closure

 

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Module 13: Research Misconduct

 

Medical Writing

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Module 1: Introduction to Medical Writing

 

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Module 2: Essential Clinical Trial Documents

 

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Module 3: Developing Standard Operating Procedures (SOPs)

 

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Module 4: Developing Clinical Trial Protocol

 

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Module 5: Developing Informed Consent Document

 

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Module 6: Developing Case Report Forms (CRFs)

 

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Module 7: Developing Data Management Plan

 

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Module 8: Developing of Clinical Study Report (CSR)

 

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Module 9: Clinical Research Glossary

 

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Assessment and Evaluation through Exam

 

How This Works?

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

Upon receipt of login details or material, the participant can read or 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 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 this course, you should be able to learn about the:

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Concepts and processes involved in clinical trials

 

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Knowledge& skills required to start your career in Clinical Research

 

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Process and Strategies to design essential clinical trial documents

 

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Hands on training and assessment through exam

 

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Roles and responsibilities of clinical research personnel.

 

Participant’s Feedback

Average Rating

100% recommend to anyone who would like to learn how to create clinical trial documents.

Prashant Dixit

Wonderful and fun learning course. A lot of insight and good applicability through the exam.

Phani Suri

I really learned a ton and hope to apply it to my current job profile.

Anil Kumar

This course goes into so much detail on just about every aspect of clinical research and medical writing.

Priyanka Mishra

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, 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 is the difference between Online and Distance learning?

In online mode of learning, you will get login access to read the course modules. You can learn anytime and from any device. In distance mode of learning, you will receive a printed/ hard copy of course material at your corresponding address via post. So, you can choose any mode of learning as per your convenience.

How can I enroll and pay the fee?

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

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