Dual Certification in Clinical Research and Medical Writing

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

  4.6 (550+ Ratings)

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Curriculum

Learning Objectives

Testimonials

FAQs

About This Course

Clinical research is a branch of healthcare science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use.

Medical writing or scientific writing of documents is a specialized skill that demands training to learn research documents drafting and designing process.

To date, more than 375000 clinical trials are registered at clinicaltrials.gov. The present estimated worth of the global clinical trial industry is 44.3 billion. ICH-GCP and regulatory guidelines provide a framework of principles that aims to ensure the safety of study subjects along with integrity and validity of data produced during trials. Both the industry offers several career options for health science professionals to advance their career for the job positions of Clinical Research Coordinator, Trial Coordinator, Research Assistance, Medical Writer, Research Nurse etc.

If you are looking to start your career in clinical research or medical writing field, the course “Dual Certification in Clinical Research and Medical Writing” will certify and train you to develop the required skills.

DCCRMW is a globally valid self-paced training course that will provide you comprehensive training on scientific, practical, ethical and technical concepts of Clinical Research and Medical Writing in compliance with global regulatory guidelines.

Who Should Enroll?

The course can be attended by:

Health-science professional (working/fresher/ student) from Pharmacy, Life-Science/ Biotech, Medicine, AYUSH (Alternate Medicine), Dental, Nursing, Physiotherapy, Ph.D. background who are looking to gain knowledge & start their career in the clinical research and/or medical writing industry.

Fresher and experienced clinical research personnel.

Rs.11200 16000  30% Off

Course Highlights

30% Discount Until 15th November

Last Day to Enroll: 30th November'24

Online and Distance

Rs. 11200 / $175 After Discount

6 Months Duration

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Single Online Exam

Global Acceptance

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Lifetime Access to Content
Immediate Access
Includes Certificate of Completion
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Approx. 100 Hours of Effort

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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

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:

Concepts and processes involved in clinical research and medical writing.

Step-by-Step process and strategies to design essential clinical trial documents.

Knowledge and skills required to start a career in clinical research and medical writing domain.

Global guidelines and standards governing clinical trials.

Hands-on training and assessment through the exam.

Testimonials

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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