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Study Director- Preclinical Safety Pharmacology with GLP and CRO Vivo Bio Tech

5.0 - 10.0 years

4 - 7 Lacs

hyderabad

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Role Overview: We are seeking a Study Director with proven experience in Safety Pharmacology to lead end-to-end studies in compliance with GLP and regulatory guidelines. The candidate should have prior CRO experience and be fully capable of independently designing study protocols, executing studies, and delivering comprehensive reports to clients. Key Responsibilities: Protocol Design: Develop scientifically sound and regulatory-compliant protocols for CNS, CVS, respiratory safety pharmacology studies, and hERG assay. Study Conduct: Oversee and ensure accurate execution of studies, coordinating with technical staff and laboratory teams. Data Analysis & Interpretation: Review raw data, perfor...

Posted 3 months ago

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