Clinical Scientist Associate Director – Late Development, Oncology

Clinical Scientist Associate Director – Late Development

What You Will Do

• Support set up and execution of late phase clinical trials with a focus on data quality.
• Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity.
• Provide input into and implementation of data management plan, CRF design, and data review oversight.
• Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission.
• Assist the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects.
• Anticipate and actively manage problems across a broad spectrum of cross-functional teams.
• Work cross‑functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protoco...