Lead scientific aspects of clinical/scientific execution of clinical protocols.
Serve as the lead Clinical Scientist on the clinical trial team.
Lead medical monitoring in review and interpretation of data and deviations.
Collaborate cross-functionally on protocol development and study materials.
Ensure CRF design supports data collection per Protocol with Clinical Data Management.
Collaborate to monitor clinical data to ensure quality, completeness, and integrity of trial conduct.

🎯 Requirements

Master's in life sciences + 3 years clinical drug development, or PhD/PharmD/RN
Solid knowledge of GCP/ICH regulatory requirements
Strong ability to manage multiple priorities and time management
Analytical skills to interpret trial data and synthesize conclusions
Proficient to propose/design studies and author docs (monitoring plan, SAPs, ICF)
Experience collaborating with stakeholders across Clinical Development

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