SESeven Consultancy
Clinical Trial Manager
Delhi ₹5-8 LPA Posted 12 Dec 2025
FULL TIME
Dentistry
Scaling
Rct
Restoration
Regulatory Affairs
+1 more
Job Description
- Perform activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions.
- Assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring site compliance with protocol requirements and study procedures.
- Create and maintain Trial Master File (TMF) and project files, including participation in file audits.
- Prepare and maintain site manuals, reference tools, and other clinical documentation.
- 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.
- Maintain awareness in the field of clinical research by completing assigned training and staying updated on industry standards.