SESeven Consultancy
Clinical Trial Associate
Bangalore ₹5-7 LPA Posted 12 Dec 2025
FULL TIME
clinical operations
Clinical Trials
Clinical Data Management
clinical monitoring
Clinical Research
Job Description
- Perform activities in compliance with corporate and clinical operations policies, SOPs, and work instructions.
- Assist Clinical Monitoring staff with site management activities; act as a Sponsor representative for assigned studies.
- Ensure sites comply with protocol requirements, study procedures, and relevant guidelines.
- Create and maintain Trial Master File (TMF) and project files, including participation in audits.
- Prepare and maintain site manuals, reference tools, and other study documents.
- Maintain, update, and input clinical tracking information into databases.
- Track incoming and outgoing clinical and regulatory documents for investigator sites, studies, project teams, or clients.
- Manage shared mailbox, process site requests, and route correspondence appropriately.
- Coordinate ordering, packaging, shipping, and tracking of site supplies and materials.
- Handle receipt, tracking, and disposition of Case Report Forms (CRFs) and queries as needed.
- Stay updated on clinical research developments by completing assigned training.