Introduction to Clinical Research
- Fundamentals of clinical research
- History and evolution,
- Current trends

Clinical Trial Design and Management
- Phases of clinical trials
- Protocol development
- Study design and methodology

Regulatory Affairs
- International regulations (FDA, EMA, etc.)
- Good Clinical Practice (GCP)
- Ethics committees and IRBs

Data Management and Biostatistics
- Data collection and management
- Statistical analysis
- Interpretation of results

Ethics in Clinical Research
- Informed consent
- Patient rights and safety
- Ethical dilemmas and case studies

Clinical Research Operations
- Site management
- Monitoring and auditing
- Quality control

Global Clinical Research
- Conducting trials in diverse populations
- Cultural considerations
- International collaborations

On-Site Training 12 Months

Duration: 12 months
Locations: Partner hospitals and research centres

Activities:
- Monitoring clinical trials
- Managing patient data
- Coordinating with research teams
- Reporting and documentation
- Quality assurance practices

Career Opportunities
Graduates of the program can pursue various roles, including:
- Clinical Research Coordinator
- Clinical Trial Manager
- Regulatory Affairs Specialist

Admission Requirements
- Educational Background: Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or related fields.
- Language Proficiency: Proficiency in English & Hindi

Application Process
1. Online Application: Complete the online application form on our website.
2. Supporting Documents: Submit transcript, Photo, Id Proof, Address Proof.
3. Interview: Attend an interview (in-person or virtual) with the admission counsellor.
4. Acceptance: Receive an admission offer and confirm your enrollment.

Fees and Financial Aid
Tuition Fee: 1.5 lakh + GST (includes online classes and on-site training)
Clear all dues before the Exams or any assissments.
Payment Plans: Flexible payment options (Quarterly / half-yearly)