Job Summary

• The role involves overseeing the planning, execution, and interpretation of clinical trials research and data collection activities.
• Candidates are responsible for establishing scientific methods for the design and implementation of clinical protocols and final reports.
• The position requires contributing to the development of clinical sections of trial documents and ensuring overall compound safety.

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Skills & Requirements

Key Requirements

• Managing crises and collaborating across boundaries
• Functional breadth in clinical trials and drug development
• People management and data analysis skills

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