Clinical Research Job at Syngene | Pharma Job Opening in Bangalore| Apply Now
Looking for an exciting Pharma job in clinical research and clinical operations? Syngene is hiring a Senior Clinical Research Associate in Bangalore under its Discovery Services division. This opportunity is ideal for professionals seeking Pharmacy Jobs in clinical trials, site management, and clinical operations. Explore this promising Syngene career opportunity and work with one of India’s leading innovation-driven
- Job Title: Senior Clinical Research Associate
- Job Location: Bangalore, India
About the Company
Syngene is a leading innovation-driven contract research and manufacturing organization providing integrated scientific services from discovery to commercial supply. Known for strong safety standards, quality compliance, and operational excellence, Syngene career opportunities are ideal for professionals seeking clinical research jobs and CRA jobs in the pharmaceutical industry.
Job Description
- Conduct site selection, site initiation, monitoring, and close-out visits for clinical studies
- Ensure clinical trial activities are performed according to study protocols, SOPs, GCP guidelines, and regulatory requirements
- Manage assigned clinical trial sites and maintain effective communication with investigators and site staff
- Monitor patient recruitment, study progress, and data quality throughout the clinical trial
- Review Case Report Forms (CRFs) and resolve data queries in coordination with study sites
- Track regulatory submissions, Ethics Committee approvals, and essential study documentation
- Identify quality issues during site monitoring and support the implementation of Corrective and Preventive Actions (CAPA)
- Prepare monitoring visit reports, follow-up letters, and other required clinical trial documentation
- Provide protocol and study-related training to site personnel when required
- Ensure timely completion of assigned project tasks and documentation activities
Key Responsibilities
- Monitor clinical trial sites for protocol compliance, data accuracy, and patient safety.
- Ensure all regulatory requirements are met and adhered to.
- Perform site management activities, including site selection, initiation, and close-out visits.
- Communicate effectively with clinical trial investigators and site staff.
Qualifications
- M. Pharm, Pharm D
- Prior experience as a Senior Clinical Research Associate (Sr. CRA)
- Knowledge of clinical trials, GCP guidelines, site management, and clinical operations
- Good communication and teamwork skills
- Strong attention to detail and problem-solving skills
Benefits
- Competitive salary and benefits package.
- Opportunities for career advancement.
- Comprehensive training programs.
