🕒 6 to 9 Months (Flexible schedule for working professionals)
🎯 100% Placement Assistance with top CROs, pharma companies, hospitals, and research organizations.
Focus on clinical trial operations, site management, ethics & regulatory affairs
Training in monitoring practices, study design, budgeting, and compliance
Ideal for professionals seeking roles in project coordination, site management, and regulatory affairs
🎓 Instructor-led Sessions: Live lectures by industry experts using case-based discussions and real-world examples
🧾 Assignments & Projects: Including protocol designing, ICFs, CRFs, site audit checklists, SOP reviews, and budgeting exercises
🧪 Simulated Workshops: Practical exposure through hands-on training and project simulations
📈 360° Evaluation System: Tracks the learner’s growth across knowledge, skills, and behavior for holistic development
Suitable for:
Graduates in Pharmacy, Life Sciences, Medicine, Nursing, or Allied Health
Working professionals in hospitals, CROs, or pharmaceutical companies
Final-year students or diploma holders with relevant experience
Examples of eligible backgrounds:
B.Pharm, M.Pharm, MBBS, BDS, BHMS, BUMS
B.Sc / M.Sc / PhD in Biotechnology, Microbiology, Biochemistry, Bioinformatics, Chemistry, Zoology
B.Sc Nursing, B.V.Sc, M.V.Sc
✍️ Resume Building Techniques
💼 Interview Cracking & Communication Skills
🚀 Navigating the First 90 Days of a New Role