Associate Director, Clinical Science

Role: Associate Director Clinical Scientist supporting clinical development of biopharmaceutical candidate drugs, primarily in oncology. Responsibilities include real-time monitoring of clinical data for quality and safety, authoring and reviewing study documents (protocols, investigator brochures), and generating clinical data outputs for internal and external stakeholders. The role involves cross-functional collaboration with data management, biostatistics, regulatory, medical affairs, and clinical operations, with an emphasis on ensuring trial integrity and compliance. Qualifications: PhD or equivalent with 5+ years or bachelor/master's with 10+ years of industry experience in clinical drug/biologics development, especially Phase I-III trials in Hematology-Oncology or rare diseases. Skills: strong organizational, data analysis, communication, and presentation capabilities; ability to influence multidisciplinary teams; experience with clinical data systems and regulatory processes. High-Value: Oncology, hematology, rare diseases; Phase I-III clinical trials; expertise in biologics or small molecules; track record in data review, protocol authoring, and regulatory interactions. Travel: up to 20%. Work Setup: not specified.