Clinical Research Associate Job at Syngene in Bangalore | BDS & MDS Graduates Apply
The Clinical Research Associate Job at Syngene is a rewarding opportunity for experienced professionals seeking growth in clinical operations. This role, based in Bangalore, is ideal for candidates exploring Syngene careers and long-term jobs in Bangalore within a globally recognized research organization focused on quality, safety, and regulatory compliance.
Job Details:
- Job Title: Senior 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. Syngene Careers offers exposure to global standards and meaningful jobs in Bangalore across clinical research and scientific domains.
Qualifications
- Education: BDS, MDS
- Experience: 3 – 9 Years
Job Description
The Clinical Research Associate Job at Syngene involves managing clinical trial sites, conducting site initiation, monitoring, and close-out visits, and ensuring studies are conducted in compliance with GCP guidelines and regulatory requirements. This role supports Syngene Careers by maintaining study quality, coordinating with sites, and contributing to successful clinical operations for jobs in Bangalore.
Key Responsibilities
- Overall adherence to safe practices and procedures of oneself and the teams is aligned
- Contributing to the development of procedures, practices, and systems that ensure safe operations and compliance with the company’s integrity & quality standards
- Driving a corporate culture that promotes an EHS mindset and operational discipline at the workplace at all times
- Ensuring the safety of self, teams, and lab/plant by adhering to safety protocols and following environmental, health, and safety (EHS) requirements at all times in the workplace
- Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team, including self
- Compliance with Syngene’s quality standards at all times
- Hold self and their teams accountable for the achievement of safety goals
- Govern and review safety metrics from time to time
- Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, generating follow-up letters, and other required study documentations
- Timely submission of timesheets for project-specific and other tasks
