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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...
Posted 4 months ago
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