Dental Job Opportunity at Syngene | Apply now
If you are searching for a rewarding dental job in clinical research, an exciting opportunity is now available at Syngene. The company is hiring a Senior Clinical Research Associate in Bangalore within its Clinical Operations division. This role offers professionals with dental and clinical research backgrounds the chance to work in a globally recognized contract research organization and contribute to cutting-edge healthcare research. If you are exploring Syngene careers, this position could be an excellent step toward building a strong career in clinical research and drug development.
Job Details:
- Job Position: Senior Clinical Research Associate
- Location: Bangalore, India
- Department: Clinical Operations – T&CR
About the Company:
Syngene is an innovation-driven contract research, development, and manufacturing organization that provides integrated scientific services from early discovery to commercial supply. The organization supports global pharmaceutical and biotechnology companies through advanced research capabilities and clinical services.
In Syngene careers, safety is considered a core principle. The company ensures that safety, quality, and compliance standards are followed across all operations. Employees are encouraged to maintain high professional standards while contributing to a culture that prioritizes environmental, health, and safety (EHS) practices.
Job Description:
The Senior Clinical Research Associate role at Syngene involves managing clinical trial sites and ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. This Clinical Research Associate job focuses on performing site selection, initiation, monitoring, and close-out visits according to the contracted scope of work.
The role requires coordination with clinical teams and research sites to maintain the quality and integrity of clinical studies. Professionals applying for this dental job will also be responsible for ensuring proper documentation, training, and adherence to regulatory standards across assigned clinical trials.
Qualifications:
- Education: BDS, MDS
- Experience: Experience working as a Senior Clinical Research Associate (Sr. CRA) is preferred.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits according to SOPs and GCP guidelines.
- Manage assigned study sites, protocols, and therapeutic areas effectively.
- Complete necessary SOP training, protocol training, and therapeutic area training required for the role.
- Provide protocol and study training to assigned sites and maintain regular communication with site teams.
- Ensure the quality and integrity of studies conducted at site level according to protocols and regulations.
- Investigate quality issues and coordinate with the Clinical Project Manager to implement corrective and preventive actions.
- Track regulatory submissions, Ethics Committee approvals, and recruitment progress.
- Monitor case report form (CRF) completion, submission, and data query resolution.
- Maintain documentation related to monitoring visits, findings, and follow-up action plans.
- Submit visit reports and follow-up letters for proper study documentation.
- Ensure timely submission of timesheets related to project activities.
Safety and Compliance Responsibilities:
Employees at Syngene are expected to follow strict safety guidelines and maintain compliance with organizational standards. Key expectations include:
- Adherence to safe practices and procedures for self and team members.
- Contribution to systems and procedures that support safe operations.
- Promotion of an environment, health, and safety (EHS) culture.
- Compliance with quality standards and integrity guidelines.
- Completion of mandatory training related to data integrity and safety.
- Monitoring and reviewing safety metrics periodically.
