Medical Director, Hematology Clinical Development

Role: Lead clinical development in oncology or hematology, overseeing the planning, execution, and interpretation of complex clinical trials aligned with product development strategies. Responsibilities: design and manage clinical programs from early translational to late-phase studies, ensure study integrity, safety, and efficacy data quality, and oversee regulatory documentation including protocols and reports. Provides scientific expertise, mentors teams, and collaborates with cross-functional stakeholders including Medical Affairs and Discovery. Ensures compliance with GCP, regulatory standards, and pharmacovigilance. Qualifications: MD or equivalent in relevant therapeutic area, with at least 2 years of industry or academic clinical trial experience. Demonstrated ability to manage moderate complexity clinical programs independently, with strong knowledge of trial methodologies, regulatory requirements, and study design. Preferred: oncology/hematology specialty, experience in global clinical development, and leadership roles in cross-functional teams. HighValue: Oncology/Hematology, clinical trial phase (early to late), regulatory compliance, cross-functional collaboration, global scope. WorkSetup: not specified; likely requires working with international teams.