KYVERNA is pioneering a new class of treatments and potential cures for serious autoimmune diseases. Backed by Insight Partners.
About the role
Serve as the senior physician for CAR T-cell therapy clinical trials in autoimmune disease indications, partnering closely with internal and external cross-functional teams. Strategically contribute to and lead clinical development plans and study execution activities for neuroimmunology, autoimmune disease, and cell therapy programs.
What they're looking for
- MD , DO, (or ex-US equivalent) required
- 5 + years of clinical research experience wit h at least 4 years of industry experience in clinical development , in cluding the design and execution of clinical trials
- Experience in late -stage clinical development highly preferred
- Specialty training in neurology, rheumatology, nephrology and/or industry experience in clinical development of cell therapies and/or therapies for autoimmune diseases highly preferred
- Proven ability to interpret, discuss and present efficacy and safety data
- Strong knowledge of GCP/ICH, clinical trial design, clinical development processes, and regulatory requirements
More about this role
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.
Position Overview
Kyverna is seeking a Sr. Medical Director, Clinical Development . This role will serve as a senior physician for CAR T-cell therapy clinical trials in autoimmune indications, providing medical oversight across study design, execution, and data interpretation. This person will p artner cross-functionally to align on clinical strategy, lead oversight of medical monitoring activities, and directly engage with investigators and key thought leaders . In addition, this person will c ontribute to the development of clinical development plans, protocols, and regulatory submissions, and will also analyz e safety, efficacy, PK, and biomarker data. In addition, this person will s upport external collaborations and...
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