Senior Medical Director

Summary

Join Recursion, a clinical-stage biotechnology company, as a Senior Medical Director in Clinical Development. You will oversee the development of first-in-class/first-in-disease molecules in precision oncology, generating and refining clinical development strategies. Responsibilities include contributing to regulatory submissions, enhancing clinical trial design, and providing medical expertise for business development. The ideal candidate possesses a Medical Degree (MD/PhD preferred), 5+ years of experience in clinical trials (ideally Phase 1/2) within biotech/pharma, and deep oncology knowledge. Remote work is considered, with regular on-site visits required. Compensation includes a competitive salary ($250,000 - $305,000), bonuses, equity compensation, and a comprehensive benefits package for US-based candidates.

Requirements

• Medical Degree
• 5+ years of experience in developing, executing and analyzing clinical trials (ideally Phase 1/2), and preferably within a biotech or pharmaceutical company
• Deep knowledge and understanding of oncology and genetic diseases; precision oncology drug development paradigms, clinical pharmacology with technical and regulatory approaches
• Strong networks and connections to external experts and key opinion leaders in oncology. Ability to form effective collaborations with external scientific community, academia and CROs
• Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders
• Highly motivated, decisive, and results-oriented individual who is proactive, resourceful, and efficient with the flexibility and creativity to excel in and contribute to a rapidly growing drug discovery and development company

Responsibilities

• Oversee the development of first-in-class/first-in-disease molecules in precision oncology
• Generate and continually refine the integrated clinical development strategy for Recursion’s oncology medicine portfolio from IND to POC
• Contribute to regulatory submissions and participate in regulatory agency meetings
• Utilize strong therapeutic area expertise to enhance innovation and efficiency in clinical trial design and execution
• Deliver medical, disease-specific, and development perspective into specific research programs or broader research initiatives
• Provide scientific and medical expertise for business development assessments and due diligences

Preferred Qualifications

MD/PhD

Benefits

• Salary: $250,000 - $305,000 (depending on experience)
• Bonuses
• Equity compensation
• Comprehensive benefits package (for US-based candidates)
• Remote work considered (with regular on-site visits)