via Career pages·1w ago
Research Associate
Cadila Pharmaceuticals
Full-timeOn-siteclinical trial coordinationregulatory compliancegood clinical practicesite initiationmonitoring plan developmentclinical study material distributioncrf managementsop preparationsite identificationfeasibility studiesdocumentation managementquality controlethics committee coordinationstakeholder communicationproject trainingproject management
Location:Dholka, IndiaType:Full-timePosted:1w ago
Embrace the opportunity to become a Clinical Research Associate and play a vital role in ensuring clinical trials meet regulatory and ethical standards. Coordinate site initiation, monitor study progress, and support project delivery in a dynamic environment. Grow your career in clinical research with hands-on experience and impactful contributions.
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