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Sr. Medical Director, Rare Disease/Oncology

Recursion Pharma

This is a Full-time position in Los Angeles, CA posted August 15, 2021.

The Impact You’ll Make Provide integrated and innovative clinical development strategy to support the creation and management of the clinical development plan for assets in development Integrate scientific rationale, regulatory requirements, clinical development plan to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP Drive end-to-end integrated clinical development strategy to achieve regulatory approvals, Generate data and evidence to determine a medicines potential efficacy, safety profile, key areas of product differentiation and value to patients in the shortest possible time frame Lead clinical development discussions at regulatory interactions and clinical components of the submissions (e.g.

IND, NDA, BLA, MAA) including briefing documents, presentations, addressing questions and responses Assess insights to inform medical strategy and to address unmet patient need in the rare disease space and broaden potential patient benefit Develop review and revise protocols The Team You’ll Join The Development Team is an empowered, execution-minded group of drug development professionals responsible for translating Recursion’s innovative science to patients through clinical development activities.

As Sr.

Medical Director, Rare Disease/Oncology, you will report to the Chief Medical Officer and serve as a key member of the Development Team.

In your role, you will work with colleagues in Development and cross-functional peers across the Recursion organization.

The Experience You’ll Need MD degree and 8 years of experience in clinical development, with at least 5 years in the biopharmaceutical industry Experience in drug development within rare disease or oncology a plus Well versed in regulatory requirements and fundamental principles of clinical trial design Expertise clinical training and/or applicable clinical research experience; understanding of clinical development planning and running clinical trial from concept study idea to publication Experience in clinical drug development with an understanding of multiple diseases, the underlying biology and potential therapeutic targets and current and future potential treatment options in all clinical trial phases Experience managing complex projects and working collaboratively with multiple stakeholders regarding new strategies to ensure timelines are met Intrinsic desire to champion innovative methods and processes within clinical development Experience with clinical research methodology and biostatistics principles, to facilitate efficient clinical trial design, and clinical development plans with clear, data-driven decision results