Medical Director

Role: Medical Director responsible for leading clinical development of CAR-T and cell therapy programs, overseeing trial design, execution, and data interpretation. Responsibilities: manage phase I-IV clinical trials, develop clinical strategies, ensure trial safety and compliance with GCP/ICH, build and lead clinical teams and CRO relationships, author regulatory documents, monitor adverse events, and support regulatory submissions. Qualifications: MD with hematology expertise, prior experience in cell therapy trials, regulatory agency interaction knowledge, excellent communication skills, and ability to work autonomously in a fast-paced environment. Nice-to-haves: experience with product launches (BLA/MAA), immuno-oncology, cell engineering, and biotech industry background. High-Value: focus on hematologic malignancies, cell therapies, clinical trial phases I- IV, regulatory interactions, experience with FDA/EMA/PMDA, and GxP compliance. WorkSetup: not specified, likely hybrid/onsite with US work eligibility.