Director, Clinical Development (MD)

Role: Medical Lead providing scientific and clinical guidance for the development of assigned biopharma molecules, primarily in autoimmune or inflammatory indications. Responsibilities include contributing to Target Product Profiles, clinical development plans, trial protocol design, and medical monitoring of phase 1 and 2 clinical trials. The role involves managing regulatory documentation, data review, and scientific presentations, ensuring compliance with GCP and industry standards. Requirements: MD or equivalent with 4+ years' experience in clinical/scientific drug development, preferably with phase 1/2 autoimmune or inflammatory disease expertise; board certification in rheumatology, dermatology, gastroenterology, or allergy/immunology is preferred. Experience in biopharma industry, leading cross-functional teams, and protocol development is advantageous. Knowledge of regulatory processes, clinical trial conduct, and GxP is essential. High-value specifics include early-phase autoimmune or inflammatory disease research, medical monitoring, and regulatory document management. Collaboration spans cross-functional teams, with a focus on scientific and regulatory excellence. The role is based within Gilead’s clinical research framework, with a focus on innovative therapeutics in infectious and autoimmune diseases.