Apply📍 United States
💸 250000.0 - 305000.0 USD per year
🔍 Biotechnology
- Medical Degree and MD/PhD preferred.
- 5+ years of experience in developing, executing and analyzing clinical trials (ideally Phase 1/2).
- 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.
- Oversee the development of first-in-class/first-in-disease molecules in precision oncology.
- Generate and continually refine the integrated clinical development strategy for the 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.
CollaborationStakeholder management
Posted about 2 months ago
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