Clinical Research Associate Job at Sun Pharma | Apply Before It’s Gone!
Looking to build a successful career in clinical research? Sun Pharma Laboratories Ltd is hiring for a Clinical Research Associate in Mumbai under its Medical Affairs & Clinical Research division. This opportunity is ideal for professionals seeking clinical research jobs in India while working with one of the country’s leading pharmaceutical companies.
About Sun Pharma
Sun Pharma is India’s largest pharmaceutical company and one of the world’s leading specialty generic pharmaceutical organizations. The company is committed to developing innovative, high-quality medicines that improve patient outcomes across global markets. Through Sun Pharma Careers, professionals gain access to world-class research, clinical development, and regulatory expertise while working in a collaborative environment that encourages innovation, continuous learning, and excellence in pharmaceutical research.
Location: Sun House – Corporate Office, Mumbai
Employment Type: Full-Time
Experience: 1–5 Years
Responsibilities
- Perform site feasibility assessments and identify suitable investigators.
- Negotiate study budgets and finalize study-related contracts.
- Prepare and submit ethics committee documentation.
- Conduct site initiation, monitoring, and close-out visits.
- Train investigators and study coordinators on protocols and Good Clinical Practice (GCP).
- Monitor investigational product accountability and inventory.
- Support participant recruitment and data verification.
- Report Serious Adverse Events (SAEs) in compliance with regulatory requirements.
- Coordinate with CROs and internal teams for study management.
- Identify study risks and implement corrective actions when required.
Requirements
- Bachelor’s or Master’s degree in a health-related discipline.
- Postgraduate Diploma in Clinical Research.
- 1–5 years of relevant experience in Clinical Research.
- Knowledge of Good Clinical Practice (GCP) and clinical trial regulations.
- Experience in clinical trial site monitoring is preferred.
Skills
- Clinical trial monitoring
- Good Clinical Practice (GCP)
- Regulatory compliance
- Clinical documentation
- Ethics Committee submissions
- Site management
- Investigator coordination
- Data verification
- Clinical Operations
- Medical Affairs
- Communication and stakeholder management
- Problem-solving and analytical skills