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3.0 - 5.0 years
4.0 - 5.0 Lacs P.A.
Hyderabad
Posted:1 week ago| Platform: 
Work from Office
Full Time
Design and execute clinical studies per medical device standards; collaborate with teams; prepare protocols and reports; liaise with CROs/sites; support regulatory submissions; maintain detailed records. Should be skilled in PCR, ELISA. Required Candidate profile Strong in molecular biology, clinical study design, protocol writing, documentation. Skilled in PCR, ELISA, and data analysis. Knowledge of clinical regulations. Good at reporting and communication.
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