What is Clinical Research?
Clinical research investigates new drugs, therapies, or medical devices directly in people to verify safety and effectiveness. It follows a structured sequence of trials that generate evidence for doctors, patients, and regulators. Volunteers enroll under strict ethical standards and oversight to protect their rights and well-being. Each trial phase answers specific questions—from initial safety to large-scale efficacy.
Results guide approval, help refine treatments, and drive continuous improvements in healthcare.
🌟 Why Enroll in This Course?
India is undergoing a transformative journey to establish itself as a global competitor, and clinical research is a key area driving this evolution. With years of involvement in clinical trials, India is rapidly emerging as a major hub for clinical research. Billion-dollar companies are already witnessing a surge in demand for skilled professionals in this domain.
The pharmaceutical industry in India is among the fastest-growing sectors of the economy, showing remarkable progress over time. As this industry expands, so does the need for qualified clinical research experts. This field offers a dynamic and rewarding career path, with numerous opportunities for advancement.
Organizations such as pharmaceutical companies, IT firms, and Contract Research Organizations (CROs) are actively recruiting professionals with clinical research expertise. Market forecasts suggest that the global clinical trials industry will reach approximately USD 174.3 billion by 2033, growing at a CAGR of 6.8% from 2024 to 2033. In addition to career growth, the field offers flexibility, remote work options, and competitive salaries.
🎓 Who Should Apply?
Applicants must have a minimum of 55% in their graduation.
Eligible degrees include:
- Medical Degrees: MBBS, BDS, BAMS, BHMS, BUMS, Pharmacology
- Life Sciences/Biosciences: B.Sc., M.Sc. in Biomedical, Biotechnology, Microbiology, Medical Lab Science
- Pharmacy: B. Pharm, M. Pharm, PharmD
- Nursing & Allied Health: BPT, OT, Nursing
🎯 Program Highlights
- Learn the entire drug development process and the phases of clinical trials
- Understand the approval process for drug marketing and manufacturing
- Conduct Bioavailability/Bioequivalence (BA/BE) studies
- Follow ICH-GCP guidelines and its 13 core principles
- Ensure compliance with Institutional Review Boards (IRBs) and informed consent protocols
🧠 Skills You’ll Gain
- Grasp the clinical research workflow, trial phases, regulatory frameworks, and distinctions between generic and branded drugs
- Master ICH-GCP principles, IRB/Ethics Committee roles, and informed consent procedures
- Build expertise in research protocols, quality control (QC), quality assurance (QA), audits, inspections, and regulatory documentation
- Learn best practices for privacy, record-keeping, and documentation in clinical trials
- Understand the responsibilities of key stakeholders like Principal Investigators (PI), Sponsors, and research teams, including strategies for participant recruitment and retention
📝 How to Apply
You can apply for the Clinical Research Certification Course directly through our website. Once your application is submitted, our team will guide you through the next steps.
Alternatively, reach out to our admissions team:
- 📞 Call Us
- MAIL : clinicaledutech@gmail.com