Syngene CRA Job Opening | Clinical Research Career Opportunity | Apply Now
Looking for an exciting Pharma Job in clinical research and clinical operations? Syngene is hiring for the position of CRA in Bangalore under its Discovery Services division. This excellent opportunity is ideal for candidates seeking Clinical Research Jobs with hands-on experience in site management, monitoring activities, and clinical operations. Explore this promising Syngene career opportunity and advance your professional journey in the pharmaceutical and clinical research industry.
- Job Title: CRA
- Division: Discovery Services
- Job Location: Bangalore
- Department: Clinical Operations
About the Company
Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
At Syngene, safety is at the heart of everything the organization does personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit.
Job Description
- Conduct site selection, initiation, monitoring, and close-out visits following GCP guidelines and SOPs.
- Manage assigned clinical trial sites, protocols, and therapeutic areas.
- Complete required protocol, SOP, and therapeutic training programs.
- Provide study-related training and maintain regular communication with assigned sites.
- Ensure study quality, compliance, and data integrity at the site level.
- Identify and discuss quality issues with the Clinical Project Manager for corrective actions.
- Track regulatory approvals, patient recruitment, CRF submissions, and query resolutions.
- Prepare monitoring reports, follow-up letters, and maintain study documentation.
- Assist in designing study tools, documents, and processes.
- Submit project timesheets and complete assigned tasks on time.
- Support coordination activities within the clinical project team.
- Handle delegated responsibilities from the Clinical Project Manager.
Key Responsibilities
- Follow all safety practices, procedures, and workplace guidelines.
- Support the development of safe operational systems and quality standards.
- Promote a strong Environment, Health, and Safety (EHS) culture in the workplace.
- Ensure safety protocols are followed in labs, plants, and work areas at all times.
- Complete mandatory training programs related to safety, health, and data integrity on time.
- Maintain compliance with Syngene’s quality and safety standards.
- Take responsibility for achieving team and workplace safety goals.
- Monitor and review safety performance and metrics regularly.
Qualification
- Master’s in Pharmacology
- Experience: Looking for a CRA with hands-on experience in core clinical research activities.
