What are the responsibilities and job description for the Senior Medical Director position at Recursion?
The Impact You’ll Make
- Lead clinical development for 1 or more clinical candidates through Phase 1-3
- Influence Recursion development program strategy by leading and/or contributing to the Target Product Profile, Clinical Development Plan, regulatory interactions
- Innovate by providing leadership, guidance, expertise to implement innovative trial designs that expedite and optimize the drug development process
- Deliver high quality clinical outputs (protocols, Investigator’s brochures, clinical study reports)
- Collaborate with internal and external stakeholders to radically rethink drug development in the service of expeditiously getting drugs to patients who need them
The Team You’ll Join
The Clinical Development Team is an empowered, execution-minded group of professionals responsible for translating Recursion’s innovative science to patients. You will be the lead clinical scientist on one or more development programs, providing both hands-on support as well as cross-functional leadership. You may also serve as medical monitor on one or more programs. You’ll collaborate within and across departments to agree on what the most important challenges and capabilities are, then figure out how to get us there. Reporting to the VP Clinical Development, you will be joining a growing clinical development team.
The Experience You’ll Need
- MD or MD/PhD, preferably with clinical experience taking care of patients; oncology training/background/experience a plus
- Strong drug development knowledge with 8 years’ experience in clinical development in a pharmaceutical or biotechnology company
- Thorough understanding of clinical development from pre-clinical phases through phase 1-3, including for orphan indications and hard-to-study indications
- Strong interpersonal and communication skills (verbal and written) bridging scientific and business needs
- Experience as a people manager in the clinical development industry
- As medical monitor you will provide medical oversight as the first line of support for clinical trials and ongoing clinical trial management
- Proven expert scientific leadership skills demonstrated in successfully executing clinical trials and programs, preparing regulatory submissions and participating in regulatory interactions; oncology expertise is a plus
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