Associate Medical Director

Role: Associate Medical Director overseeing clinical development programs for targeted oncology therapies, guiding trial design, safety oversight, and cross-functional collaboration. Responsibilities: lead clinical strategy from Phase I to pivotal registration studies, manage medical oversight for trials in relapsed refractory multiple myeloma, support regulatory filings, and foster relationships with investigators, opinion leaders, and regulators. Requirements: M.D. or equivalent with 1+ years' clinical research experience in biotech, pharma, CRO, or academia; strong communication, collaboration, and problem-solving skills; ability to work in fast-paced, matrix environments. Preferred: experience in oncology/hematology, clinical operations, pharmacovigilance, and companion diagnostics. HighValue: oncology/hematology, relapsed refractory multiple myeloma, early-phase to registration studies, regulatory interactions, cross-disciplinary team leadership, external stakeholder engagement. WorkSetup: not specified; likely hybrid or remote based on typical industry standards.