Sun Pharma is one of the largest pharmaceutical companies in India and a leading global specialty generic player. With a strong presence in over 100 countries, Sun Pharma is known for its innovation, high-quality medicines, and commitment to improving healthcare. The company has a robust R&D division, making it a preferred employer for professionals in clinical research and drug development.
Job Description: Clinical Research Associate (CRA)
Key Responsibilities:
✔ Site Feasibility & Selection: Identify potential investigators, negotiate study budgets, and finalize study sites.
✔ Regulatory Submissions: Prepare and submit study documents for Ethics Committee (EC) approval.
✔ Clinical Trial Monitoring: Oversee site initiation, monitoring, and close-out activities.
✔ Investigator Training: Train site personnel on study protocols, GCP (Good Clinical Practice), and procedures.
✔ Patient Recruitment & Data Management: Ensure timely participant enrollment, data entry, and query resolution.
✔ Safety Reporting: Manage SAE (Serious Adverse Events) and SUSAR (Suspected Unexpected Serious Adverse Reaction) reporting as per regulatory guidelines.
✔ Risk Management: Identify risks, analyze deviations, and implement CAPA (Corrective and Preventive Actions).
✔ Coordination with CROs: Collaborate with CRO partners for data management, statistical analysis, and database lock (DBL).
Eligibility Criteria:
Education:
- UG: B.Pharma / B.Sc in any specialization
- PG: M.Pharma / M.Sc in any specialization
- Preferred: Post-graduate Diploma in Clinical Research
Experience:
- 1-5 years in Clinical Research (CRA experience preferred)
Skills Required:
- Knowledge of GCP, ICH guidelines, and clinical trial protocols
- Strong communication, negotiation, and site management skills
- Ability to multitask and work in a fast-paced environment
How to Apply?
📍 Locations: Mumbai, Pune, Chennai. Kolkata, Bhubaneswar, Delhi
Application Link For CRA For Mumbai, Pune, Chennai – Click Here
Application Link For CRA For Kolkata, Bhubaneswar, Delhi – Click Here
