Senior Clinical Research Associate
Experience:
6–8 yrs (oncology monitoring mandatory)
Qualification:
M. Life Sciences / M. Pharm / Pharm D
Job Location:
Ahmedabad (Hybrid)
Role:
Manage end-to-end site activities, ensure compliance with protocol, SOPs, GCP, and regulatory requirements with good communication skills for Ahmedabad location
Job Responsibilities:
- Site management, monitoring visits (SQV, SIV, IMV, COV), SDV/SDR, CRF review, IP accountability
- Support PM with project plans, site communications, newsletters
- Close-out visits, data query resolution, TMF maintenance
- Safety, regulatory coordination, investigator meetings, DSMB/CEC liaison
- Train/mentor junior staff; support audits and QMS compliance