Clinical Research
Gain in-depth knowledge of clinical trial design, GCP guidelines and trial management.
Overview
This program equips students with a thorough understanding of clinical trial phases, ICH-GCP guidelines, protocol development, informed consent processes, trial monitoring and regulatory submissions. Training covers the roles of CRA, CRC and clinical trial coordinators, preparing graduates for careers with CROs, pharmaceutical companies and hospital-based research units.
Eligibility
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences Graduates
- Freshers and working professionals
Course Duration
4 Months (Weekday & Weekend batches available)
Career Opportunities
- Clinical Research Associate (CRA)
- Clinical Research Coordinator (CRC)
- Clinical Trial Assistant
- Site Management Associate
- Regulatory Submission Executive
Training Features
- ICH-GCP certification preparation
- Protocol writing and case report form practice
- Site visit simulation and monitoring exercises
- Guidance from industry-experienced trainers
- Placement assistance with CROs and hospitals
Enquire About Clinical Research
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