Fellowship in Clinical Research for Doctors, MBBS Online - MJGH

Fellowship in Clinical Research

5.0
Course Description

Fellowship in Clinical Research: Advancing Careers in Medical Innovation

A Fellowship in Clinical Research is a specialized postgraduate program designed for healthcare professionals, researchers, and graduates from life sciences, medicine, or pharmacy who aspire to build a career in the field of clinical research. This program provides in-depth knowledge and hands-on training in the design, conduct, monitoring, and management of clinical trials and research studies that evaluate the safety and efficacy of medical treatments, drugs, devices, and procedures.

Overview of Clinical Research

Clinical research is a vital component of medical science that focuses on improving patient care by testing new interventions and comparing them with existing treatments. It follows rigorous protocols and ethical standards to ensure the reliability of results and the safety of participants. As healthcare continues to evolve, the demand for skilled professionals in this field has grown significantly, creating numerous opportunities for trained experts.

Objectives of the Fellowship

The main goal of a Clinical Research Fellowship is to develop professionals who are well-versed in clinical trial methodologies, regulatory requirements, data management, biostatistics, ethics, and Good Clinical Practice (GCP). Fellows gain an understanding of how research is conducted in various phases, from early-phase trials (Phase I) to post-marketing studies (Phase IV).

  • Clinical Trial Design and Management
    Understanding different types of clinical studies, protocol development, and trial execution.

  • Regulatory Affairs and Compliance
    Learning about national and international guidelines, including ICH-GCP, FDA regulations, and ethical considerations.

  • Biostatistics and Data Analysis
    Basics of statistical methods used in analyzing clinical trial data.

  • Pharmacovigilance and Drug Safety
    Monitoring and reporting adverse drug reactions and ensuring patient safety.

  • Medical Writing and Documentation
    Preparation of research protocols, informed consent forms, clinical study reports, and publications.

  • Project Management
    Managing budgets, timelines, teams, and resources effectively within a clinical trial.

Career Prospects

Graduates of a Clinical Research Fellowship can pursue various roles such as:

  • Clinical Research Associate (CRA)
  • Clinical Trial Coordinator
  • Regulatory Affairs Specialist
  • Medical Writer
  • Data Manager
  • Pharmacovigilance Officer
  • Project Manager in Clinical Trials

These roles are highly sought after in pharmaceutical companies, CROs, biotech firms, academic research institutions, and regulatory bodies worldwide.

Course Highlight

Modules Comprehensive modules covering various aspects of nutrition & dietetics.

Assessments Quizzes, assignments to test your knowledge and skills.

Certification Certified Nutritionist credential upon completion.

Key Features
Industry-Aligned Curriculum

Our program is designed in collaboration with industry experts to ensure you gain practical, up-to-date knowledge in clinical trial design, regulatory affairs, pharmacovigilance, biostatistics, and GCP guidelines.

Expert Faculty and Mentorship

Learn from highly qualified professionals with years of experience in clinical research, pharmaceutical development, and academic research.

Hands-On Training

We believe in experiential learning. Our fellowship includes practical exposure through internships, live case studies, and project work with reputed CROs, hospitals, and pharmaceutical companies—bridging the gap between theory and practice.

Flexible Learning Modes

Whether you're a working professional or a full-time student, our flexible course formats—including online, hybrid, and weekend batches—ensure you can balance your education with other commitments.

Placement Assistance

We don’t just train you—we help launch your career. Our dedicated career support team provides resume building, interview preparation, and access to placement opportunities with leading organizations in clinical research and healthcare.

Global Recognized Certification

Our fellowship certification is widely recognized by employers in the clinical research industry, both nationally and internationally. I

Strong Alumni Network

Our community offers ongoing support, networking opportunities, and career collaboration.

Affordable and Value-Driven

We offer high-quality education at competitive pricing, ensuring that you receive the best return on your investment. Scholarships and installment payment options are also available for eligible candidates.

Commitment to Excellence

Our mission is to empower future clinical research professionals with the knowledge, confidence, and skills needed to excel in a fast-evolving healthcare environment. We focus on quality, innovation, and ethical practices throughout your learning journey.

Course Structure

  • Clinical Research Industry
  • Difference between Clinical Research and Clinical Trials
  • Clinical Research Terminologies
  • General Medical Terminologies

  • Basics of Pharmacology
  • Pharmacodynamics
  • Pharmacokinetics
  • Routes of Administration
  • Dosage forms

  • Drug discovery
  • Target Identification
  • Lead Identification
  • Lead Optimization
  • Preclinical studies

  • Evolution of Ethical and Regulatory Framework
  • Nuremberg Code, 1946
  • Declaration of Helsinki
  • Thalidomide Tragedy
  • Belmont Report
  • Schedule Y, Drugs and Cosmetics Act 1945

  • History of ICH
  • ICH Guidelines
  • ICH GCP- E6 R2
  • ICMR Ethical Guidelines
  • Ethics on use of Placebo in Clinical Trials

  • CDSCO, India
  • ICMR, India
  • USFDA, USA
  • EMEA, Europe
  • MHRA, UK
  • TGA, Australia

  • Investigator
  • Sponsor
  • Contract Research Organization (CRO)
  • Clinical Research Coordinator (CRC)
  • Clinical Research Associate (CRA)

  • Defining the Research Problem
  • Sampling Design
  • Hypothesis testing
  • Parametric and Non parametric test
  • Scientific Writing

  • Diagnostic and Treatment Trials
  • Interventional and Observational studies
  • Case control and Cohort studies
  • Randomized controlled trials
  • Quasi experiments

  • Essential Documents before, during and after the trial ICH GCP
  • Protocol
  • Informed Consent Documents
  • Investigator’s Brochure
  • Case Report Form
  • Clinical Study Report

  • Introduction to data management
  • Electronic Data Records
  • E-CRF & Interactive Web Response Systems
  • Database locking and unlocking
  • Good Documentation Practices

  • Adverse Drug Reaction
  • Serious Adverse Events (SAE)
  • SAE Reporting timelines
  • Pharmacovigilance methods
  • Signal Detection and Data Mining
  • PvPI
  • Risk Management Plan

  • Introduction to Quality Management System
  • Quality Assurance
  • Quality Control
  • Audits and Inspection
  • Types of Audits
  • General Audit Observations

  • Pharmacoepidemiology- Methods
  • Clinical Application of Pharmacoepidemiology
  • Principles of pharmacoeconomic analysis
  • Pharmaceutical Outcomes evaluations

  • Medical Devices Rules, 2017
  • Classification of Medical Devices
  • Materiovigilance
  • Phases of Medical Device Clinical Trials

  • Case reports
  • Article writing
  • Designing Clinical Trial protocol
  • CRF Designing
  • Informed Consent Documents
  • Clinical Study Reports

  • E-Consent (Audio visual consent)
  • E-Patient Reported Outcomes (e-PRO)
  • IWRS
  • Telemedicine
  • Patient e Diaries
  • Remote Patient Monitoring

  • ICH-GCP_E6 R3
  • NDCT Rules: 2019 & its Amendment (2023)
  • ICMR-HMSC
  • Recent CDSCO Notices
  • NABH Ethics Committee Standards, etc.)
Eligibility
  • MBBS / BDS / BAMS / BHMS / BPT / BUMS
  • Nurses, Pharmacists, Physiotherapists, Optometrists, and other paramedical staff
  • B.Sc. / M.Sc. in Life Sciences, Biotechnology, Microbiology, Biochemistry, Genetics, etc.
  • B.Pharm / M.Pharm / Pharm.D
  • BDS / MDS (Dentists)
  • Veterinary graduates (B.V.Sc & A.H)
  • Postgraduates in Public Health (MPH), Psychology, and Health Administration
Course Fee

Course Fee ₹120,000.00

Registration Fee ₹10,000.00


Total Fee ₹100,000.00

Our instructors are in the process of being updated to provide you with the best learning experience. We’ll have more information for you shortly—thanks for your patience!
Fellowship in Clinical Research
Enroll Now
This course includes:
Levels
Fellowship Program
Duration
12 Months
Mode
Online
Certificate
Certificate of completion

₹130,000.00

₹100,000.00
(including registration fees of 10,000.00)

Why Choose Us

Because your growth deserves nothing but the best in medical education.

Expert-Driven Curriculum
Expert-Driven Curriculum

Our program is designed in collaboration with leading healthcare professionals to ensure you receive the most up-to-date and relevant education.

Flexible Learning Environment
Flexible Learning Environment

Access course materials online anytime, allowing you to balance your studies with your professional and personal commitments.

Comprehensive Support
Comprehensive Support

Benefit from continuous support from experienced tutors and academic advisors dedicated to your success

Interactive Learning
Interactive Learning

Engage with a variety of interactive learning tools, including real-life case studies, practical assignments, and virtual simulations.

Networking Opportunities
Networking Opportunities

Connect with a diverse community of learners and professionals, providing valuable networking opportunities and peer support

Affordable Education
Affordable Education

We offer competitive pricing with flexible payment plans and financial aid options to make your education more accessible.

Recognized Certification
Recognized Certification

Obtain a certification that is respected and recognized in the healthcare industry, enhancing your professional credentials and career prospects

Career Support
Career Support

Beyond education, we provide comprehensive career guidance, job placement assistance guarantee, and ongoing professional development support.

What Our Allumini Saying

Discover How MedJoin Global Healthcare Is Transforming Careers Worldwide.

Enrolling in the Fellowship in Clinical Research with Medjoin has been a fantastic experience. The program is comprehensive, practical, and well-structured. I highly recommend it to anyone looking to advance in clinical research.

Dr. Shabnam
Dr. Shabnam
feedback

Pursuing the Fellowship in Clinical Research with Medjoin has been a great experience. The program is informative, hands-on, and thoughtfully designed. I highly recommend it to anyone aiming to excel in clinical research.

Dr. Tarini Gupta
Dr. Tarini Gupta
feedback

Doing the Fellowship in Clinical Research with Medjoin is an excellent experience. The training is insightful, practical, and well-structured. Highly recommend it for anyone looking to grow in clinical research.

Dr. Rehman
Dr. Rehman
feedback

Frequently Asked Questions

Fellowship in Clinical Research is a specialized program designed to equip healthcare professionals and life science graduates with the knowledge and skills required to conduct, manage, and monitor clinical trials and research studies.

  • Clinical trial design and methodology
  • Good Clinical Practice (GCP) guidelines
  • Regulatory affairs (FDA, ICH-GCP)
  • Biostatistics and data management
  • Pharmacovigilance
  • Ethics in clinical research
  • Project and site management
  • Medical writing and documentation

Yes, fellowships are designed in alignment with industry standards and are recognized by clinical research organizations, pharmaceutical companies, and healthcare institutions.

  • Clinical Research Associate (CRA)
  • Clinical Trial Coordinator
  • Regulatory Affairs Officer
  • Pharmacovigilance Associate
  • Medical Writer
  • Data Manager
  • Project Manager in clinical trials

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