From Science to Impact: Program at a Glance
Do you know how new medicines, vaccines, and medical devices make it safely to the market?
The answer is Clinical Research. It's the science of testing these innovations in humans to ensure they are safe and effective before reaching hospitals or pharmacies.
This program trains you to master the entire clinical research lifecycle, including study design, regulatory compliance, data management, and reporting, while gaining hands-on experience with industry-standard software like MedDRA and Veeva Vault.
You will get to work on real-world projects. Build a portfolio that impresses top pharma, biotech, and CROs. Become job-ready to shape therapies, influence healthcare decisions, and make a global impact.
Why Choose This Career
₹12–20 LPA
Salary range for Clinical Research roles in India and it increases with higher grade
$60+ Billion
Global Clinical Research market size by 2030, expected to grow steadily
12-15% CAGR
Projected growth in clinical trials and outsourced research in India
Programme Highlights
How This Course Will Launch Your Clinical Research Career
Become Industry-Ready
Learn the skills to handle clinical trials, data management, regulatory submissions, and reporting
Hands-On Projects
Work on real-world studies and simulations to build a portfolio that impresses employers
Master Key Tools
Get practical experience with MedDRA, Veeva Vault, and other essential clinical research software
Learn from Experts
Guidance from experienced clinical research professionals through every stage of trials
Global Career Opportunities
Open doors to roles in India and abroad, from CRA to Medical Writer or Regulatory Affairs Specialist
Career Support
Resume building, LinkedIn optimization, mock interviews, and placement assistance
Eligibility Criteria
Find out if you're eligible to join the next generation of clinical researchers
- ✓ Medicine: MBBS, MD, MS
- ✓ Pharmacy: B.Pharm, M.Pharm, Pharm.D
- ✓ Dentistry: BDS, MDS
- ✓ Life Sciences / Biotechnology / Microbiology / Biochemistry: B.Sc, M.Sc, PhD
- ✓ Ayurveda / Homeopathy: BAMS, BHMS
- ✓ Nursing & Allied Health Professionals
Career Path / Job Opportunities
| Role | Description |
|---|---|
| Clinical Research Coordinator (CRC) | Works at hospital or trial sites, managing day-to-day study activities |
| Clinical Research Associate (CRA) – Junior / Associate | Monitors ongoing clinical trials under supervision for accuracy and safety |
| Clinical Trial Assistant (CTA) | Provides administrative and documentation support to CRAs or Project Managers |
| Project Associate / Clinical Operations Assistant | Supports project managers and sponsor teams with trial operations |
| Clinical Research Executive / Analyst | Handles operational tasks at pharma companies or CROs |
Top Recruiters
IQVIA
Parexel
Syneos Health
PPD
Novartis
Accenture
TCS
Covance
Course Faculty Panel
This program is led by Dr. Akram Ahmad, Founder and CEO, PhD in Medicine from the University of Sydney, Australia. A globally recognized healthcare and academic leader with 14+ years of experience across India, Malaysia, and Australia. He is supported by a distinguished international panel of Pharmacovigilance and Drug Safety experts from academia, pharma, and consulting, delivering real-world insights and hands-on learning to make you job-ready for global drug safety physician and pharmacovigilance roles.
Dr Akram Ahmad
BPharm, PharmD, PhD (University of Sydney)
Capstone Project
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Clinical Trial Simulation – Design a mock trial with protocols, endpoints, and case report forms
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Data Management Project – Enter, clean, and analyze trial data using EDC tools
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Regulatory Submission Exercise – Prepare essential documents for ethics committees and regulatory approval
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Site Monitoring & Reporting – Conduct virtual site visits, identify deviations, and generate monitoring reports
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Clinical Research Report – Draft a study report or manuscript summarizing trial findings
Become Job Ready With Academically
Success in Clinical Research requires not just knowledge, but also practical skills, attention to detail, and confidence to work in global pharma and CRO environments. Our Postgraduate Certificate in Clinical Research - Job Ready Program offers:
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Professional Skills Training: Communication, email etiquette, and stakeholder coordination
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Analytical Thinking: Data interpretation, trial results analysis, and reporting insights
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Hands-On Tools Training: MedDRA, Veeva Vault, CTMS, and portfolio-building exercises
Programme Modules
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Introduction to Clinical Research & Trial Design
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Clinical Data Management & Analysis
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Regulatory Compliance & Ethics
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Pharmaceutical Research & Drug Development
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Good Clinical Practice (GCP) Guidelines
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Clinical Trials & Statistical Methods
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Clinical Research Technology & Tools
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Research Communication & Reporting
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Capstone Project & Portfolio Development
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Career Development & Soft Skills
Programme Certificate
Earn the Postgraduate Certificate in Clinical Research by Academically Global after successful completion of the programme.
This certificate validates your expertise in clinical research, trial design, regulatory compliance, data management, and GCP guidelines. These are key skills highly sought after across pharmaceutical, biotech, and CRO sectors.
Qualifying this certificate course will significantly enhance your credibility for roles such as Clinical Research Coordinator, Clinical Research Associate, Clinical Trial Assistant, and Clinical Research Analyst, equipping you to manage clinical trials with precision and regulatory compliance in the global healthcare ecosystem.
Lessons
Students
