Director, Clinical and Translational Development
NateraFull Time
Senior (5 to 8 years)
Candidates must hold an MD or MD/PhD degree with a minimum of six years of industry experience in clinical development within a pharmaceutical or biotechnology company. They should possess deep experience in early-stage development programs, including pre-IND and IND stages, with a strong understanding of clinical trial methodology, regulatory and compliance requirements, and experience in developing clinical strategy and study protocols.
The Senior Director, Clinical Development will design and oversee early-phase clinical studies for assigned portfolio companies, translating preclinical data into clinical trial design and execution. They will support the design and implementation of clinical development plans, maintain clinical and scientific expertise, review and assess adverse events, drive go/no go decisions based on safety signals, oversee medical monitoring of ongoing trials, provide medical guidance to clinical research sites, train site staff, and address investigator questions.
Develops allogeneic gamma delta T cell therapies
Adicet Bio develops cancer therapies using allogeneic gamma delta T cell therapies, which are immune cells designed to target and destroy cancer cells. Their approach utilizes donor-derived cells that are readily available, allowing for faster treatment compared to traditional methods that require a patient's own cells. The company focuses on serving healthcare providers, hospitals, and research institutions involved in cancer treatment. Adicet Bio's business model includes developing and commercializing its proprietary therapies, generating revenue through product sales and licensing agreements. A recent merger with resTORbio aims to enhance their technology and accelerate development. With significant funding, Adicet Bio is dedicated to improving cancer treatment outcomes through its unique immunotherapy approach.