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10.0 - 12.0 years
8 - 11 Lacs
bengaluru
Work from Office
Lead technical team, ensure evaluations, compliance, fraud checks, vendor management, audits, and policy monitoring. Coordinate with legal, maintain MIS, drive productivity. Education :Civil BE/BTech, 10–12 yrs exp Willing to travel as role demands
Posted 3 weeks ago
0.0 - 4.0 years
0 Lacs
nashik, maharashtra
On-site
As a Clinical Research Associate, your responsibilities will include developing and reviewing study protocols and informed consent documents, monitoring clinical trial progress to ensure adherence to GCP, FDA, and IRB regulations, collecting, managing, and analyzing clinical data, preparing regulatory submissions and study reports, and collaborating with cross-functional teams including investigators and coordinators. This is a full-time position suitable for freshers. The benefits include health insurance. The work schedule is during the day shift and the work location is in person.,
Posted 2 months ago
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