Medical Director, Clinical Development
Kyverna is seeking a highly motivated Medical Director with experience in clinical development to join our team developing novel and innovative engineered T cell-based therapies for autoimmune diseases. The ideal candidate will contribute to our goals of navigating what’s next in synthetic biology, immunology and cell engineering while living our core values: Bring Intellectual Rigor, Elevate Each Other, and Stay True To Why. Title: Medical Director, Clinical Development Location: Remote EligibleReports To: Chief Medical and Development Officer
Responsibilities:
- Serve as the medical lead for CAR T-cell therapy clinical trials in multiple autoimmune disease indications, in partnership with internal and external cross-functional teams.
- Support, as the clinical representative, the transition of preclinical projects to clinical development.
- Medical monitoring of clinical trials.
- Medical review, analysis, and interpretation of safety, efficacy, and PK and biomarker data.
- Development of clinical trial documents including protocols, ICFs, clinical development plans, and publications.
- Lead the development of clinical sections of regulatory documents including the IB, safety updates, clinical study reports, and responses to Health Authorities.
- Actively engage with external investigators and researchers to identify, evaluate, and support investigator sponsored studies and drive research collaborations.
Requirements:
- MD (or ex-US equivalent) or MD-PhD degree required. Advanced degree or research experience in immunology preferred.
- 3+ years of clinical research experience with 2+ years of industry experience in late phase clinical development involved in the design and execution of clinical trials. Experience in late clinical development preferred.
- Specialty training in neurology, rheumatology, nephrology and/or industry experience in clinical development of therapeutics in autoimmune diseases is highly preferred.
- Proven ability to interpret, discuss and present efficacy and safety data.
- Working knowledge of GCP/ICH, clinical trial design, clinical development processes, and regulatory requirements.
- Strong ability to communicate and establish effective working relationship with investigators, collaborators, scientific advisors, CROs, and corporate partners.
Originally posted on Himalayas
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