Clinical Research Job at Sun Pharma
Are you searching for a high-growth Clinical Research Job in India’s leading pharmaceutical sector? This is a fantastic opportunity for life science graduates to join Sun Pharma as a Clinical Research Associate and work on real-world clinical trials. If you are passionate about clinical research, patient safety, and regulatory processes, this role offers the perfect platform to build a rewarding career.
About the Company
Sun Pharma Laboratories Ltd fosters a growth-oriented environment where individuals are encouraged to take ownership of their careers, continuously improve, and collaborate effectively. The organization emphasizes personal development, leadership, and teamwork under its philosophy of “Create Your Own Sunshine.”
Job Details:
- Job Title: Clinical Research Associate
- Location: Mumbai
- Company: Sun Pharma Laboratories Ltd
- Office: Sun House – Corporate Office
Role Overview
The Clinical Research Associate (CRA) is responsible for managing and overseeing clinical trial activities across multiple sites. The role ensures that studies are conducted in compliance with regulatory requirements, company policies, and Good Clinical Practice (GCP) guidelines, while maintaining high standards of data quality and participant safety.
Key Responsibilities
- Conduct site feasibility assessments and identify potential investigators
- Negotiate study budgets and finalize investigators, sites, and contracts (including CDA execution)
- Prepare and submit study documents for Ethics Committee (EC) approvals across sites
- Oversee investigational product (IP) dispensing, inventory management, and reconciliation
- Ensure timely site initiation, monitoring, and close-out activities, along with proper documentation and reporting
- Train investigators and site personnel on study protocols, procedures, and GCP guidelines
- Monitor participant recruitment and ensure accurate data entry, source data verification, and query resolution
- Ensure timely reporting of SAEs and SUSARs in compliance with regulatory requirements and pharmacovigilance policies
- Identify risks, perform analysis, and implement corrective and preventive actions (CAPA) for underperforming sites
- Coordinate with internal teams or CRO partners for data management, statistical analysis, and database lock (DBL)
Candidate Profile
The ideal candidate is detail-oriented, proactive, and capable of managing multiple clinical trial activities while ensuring compliance and quality standards.
Educational Qualification
- Bachelor’s or Master’s degree in a health-related field such as Biology
- Postgraduate Diploma in Clinical Research (preferred)
Experience
1 to 5 years of relevant experience in Clinical Research.
