Scientific Director / Senior Medical Director, Multiple Myeloma (International Medical Affairs)

Role: Scientific Director / Senior Medical Director providing medical and scientific input into strategic medical affairs activities such as data generation, clinical study oversight, safety monitoring, and medical education. Responsibilities include designing and interpreting clinical protocols, overseeing clinical studies, ensuring regulatory compliance, developing medical strategies, supporting product launches, and coordinating cross-functional activities across clinical, regulatory, and commercial teams. Requirements: Advanced degree (PhD, PharmD, MD), with 10-15 years industry experience for Scientific Director, or 2+ years clinical/trial experience for Senior Medical Director; extensive expertise in therapeutic areas like multiple myeloma or related fields; knowledge of clinical trial methodology, data analysis, and regulatory standards; strong leadership and communication skills. HighValue: Emphasis on oncology, clinical development, global medical affairs, regulatory compliance, and collaborative cross-functional engagement. WorkSetup: Hybrid (3 days onsite) from Mettawa, IL or Florham Park, NJ; other US locations considered.