Clinical Scientific Expert I

• 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).