1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.50 LPA
Job Responsibilities:
Site monitoring, source verification, query resolution & ensuring protocol compliance
Visit investigator sites for initiation, monitoring & close-out activities
Support eTMF, CTMS, EDC documentation and trial coordination
Track patient recruitment, AE/SAE reporting, IP accountability, and site communications
Required Qualification:
B.Pharm / M.Pharm / MSc Clinical Research / Life Sciences
1–3 years CRA experience in CRO ...