Join our international team and support regulatory aspects of clinical research projects. You'll help streamline communication, manage documents, and maintain key systems - all while learning from experienced regulatory professionals.
Office-Based in Bangalore, India
What You'll Do:
- Communicate with project teams on regulatory matters and serve as a support contact for PSI services
- Maintain departmental tracking systems and regulatory calendars
- Support the preparation of regulatory submissions and license applications under supervision
- Perform quality control on outbound documents and manage filing with Document Management Systems
- Translate regulatory documents as needed
- Provide technical assistance with regulatory feasibility research
- Train PSI staff on departmental software and provide administrative support to the Regulatory Affairs team
