Clinical Scientific Expert I Thepharmadaily

1.0 - 4.0 years

3 - 7 Lacs

Hyderabad, Telangana, India

On-site

Ensure high-quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCTT). Perform thorough clinical data review and identify insights through patient-level review and trends analysis, supporting Interim Analysis, Database, and Post Lock activities. Contribute to the development of the Data Review/Quality Plan (DRP/DQP) and data review strategy. Support the development of study-level documents and contribute to pharmacovigilance activities if required. Produce training materials and provide training to iCTT. Role Requirement: Education: Advanced degree in life sciences/healthcare (or clinically relevant degree) required. Experience: >1 year experience in pharmaceutical industry/clinical research organization preferred. Skills: Strong analytical skills, knowledge of clinical trial design, statistical analysis, and regulatory processes. Fluent in English (oral and written).

Posted 5 days ago

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