What are the responsibilities and job description for the Director of Oncology Logistics position at Tempest Therapeutics?
Oncology Clinical Trials
The Associate Director of Clinical Supply will be responsible for developing and executing clinical supply strategies for oncology clinical trials. This includes ensuring alignment with trial protocols, regulatory requirements, and company objectives.
This position will require strong understanding of GMP, GCP, and other relevant regulations as well as experience in vendor management and risk mitigation.
Key Qualifications
To be successful in this role, you will need:
- Bachelor's degree in a scientific or related field. Advanced degree preferred.
- Minimum of 8 years of experience in clinical supply chain management, with a focus on oncology clinical trials.
- Demonstrated experience in developing and executing clinical supply strategies.
- Strong analytical and problem-solving abilities.
