Medical Director

Role: Medical Director, Clinical Development, leading hematology-focused clinical programs, with a primary focus on iron metabolism. Responsibilities include providing scientific leadership across clinical trial design, execution, medical monitoring, and strategy development; serving as a medical interface with cross-functional teams; supporting regulatory submissions and interactions; and contributing to scientific communications and external engagement. The position involves oversight of safety and data interpretation, as well as fostering relationships with investigators and KOLs. Requirements: MD, MD/PhD, DO, or equivalent; 3-5+ years in clinical research or development within biopharma, CRO, or academia; experience in hematology, anemia, or iron metabolism, with strong knowledge of trial methodology, safety, and efficacy data. Preferred qualifications include board certification in Hematology/Oncology or related fields, fellowship training, and experience with regulatory processes. High-value specifics: early to mid-stage clinical development programs targeting hematologic diseases, with a focus on iron metabolism; involvement in clinical trial design, safety monitoring, and regulatory documentation; approximately 20-25% travel required. Collaboration spans Clinical Science, Operations, Regulatory, Biostatistics, and Medical Affairs, with an emphasis on scientific rigor, patient safety, and ethical standards.