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Torrent Pharmaceuticals is seeking a capable Clinical Research Associate (CRA) to support study start-up, site management and monitoring across multiple sites in India. The role includes coordinating site initiation, training staff, and ensuring patient recruitment and retention.
You will manage study supplies, vendor relations, and project timelines while collaborating with cross-functional teams. Willingness to travel 20–25 days per month is essential.
Study start-up: Site feasibility assessment, Site evaluation/selection, Site / Investigator financial & study contract execution, Prepare EC submission packages.
Qualification - M. Pharm/ Pharm D
Experience - having worked as CRA