Clinical Development Medical Director (Biotechnology / Oncology)

Role: Lead clinical trial execution for oncology products, focusing on design, protocol development, safety monitoring, and data interpretation across early and late stages. Responsibilities: act as medical monitor, support study design, ensure regulatory compliance, analyze safety data collaboratively with safety teams, and interact with investigators and key opinion leaders to align scientific strategies. Requirements: MD with at least 5 years post-residency experience, with expertise in oncology or hematology/oncology; industry or academic drug development experience, particularly in controlled oncology trials involving molecular targeted or immunological therapies; strong understanding of molecular biology, immunology, or genetics; proven ability to work cross-functionally and communicate effectively. HighValue: oncology, clinical trial design and management, safety monitoring, molecular targeted/immunological therapies, regulatory compliance, GCP. WorkSetup: not specified, but collaboration with internal teams and external investigators implied.