Medical Director (MD), Multiple Sclerosis, Basel

Position Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing late-stage development (Phase II–III) clinical strategies that deliver medically differentiated therapies for patients. We are seeking a highly motivated

Medical Director

to join our Neuroimmunology team, specifically focusing on Multiple Sclerosis (MS). This is a junior to mid‑level individual contributor position without people management responsibilities.

Opportunity As a Medical Director, you will participate in or lead the development of Clinical Development (CD) plans, ensuring the effective execution of strategies for assigned molecules and indications.

CDP Strategy and Planning: Lead or contribute to the creation of the Clinical Development Plan (CDP), gathering data to ensure strategic alignment with long‑term lifecycle plans.

Study Design and Execution: Lead the design and execution of Phase II and III clinical studies, collaborating with cross‑functional teams on study analytics, data management, and safety profiles.

Scientific Leadership: Maintain the highest levels of scientific and clinical knowledge within the MS and Neuroimmunology therapeutic areas.

Regulatory Engagement: Take an active role in Health Authority (HA) interactions and provide clinical expertise for regulatory filings, briefing packages, and labeling.

Stakeholder Collaboration: Build and cultivate relationships with clinical investigators, Key Opinion Leaders (KOLs), and internal partners across research, commercial operations, and legal.

Medical Monitoring: Act as a medical monitor for assigned studies, ensuring the correct interpretation of medical and scientific data.

Qualifications

Academic&Clinical Expertise: M.D. required with relevant clinical experience as a Neurologist, including specialized training or a significant background working with Multiple Sclerosis patients.

Scientific&Industry Experience: Strong scientific background (publishing in peer‑reviewed journals, academic, or teaching background is a plus) alongside preferred prior industry experience in MS clinical development (>2 years) or recognition as an MS field expert (e.g., Assistant Professor).

Clinical Trials&Regulatory Knowledge: Significant experience designing/conducting clinical trials, a strong understanding of Phase II–III drug development, and required knowledge of GCP, ICH, FDA, and EMA guidelines (preferred for entry‑level candidates).

Communication&Interpersonal Skills: Outstanding written and verbal communication skills to present complex data, paired with the ability to build relationships and influence without authority in a complex, cross‑functional environment.

Strategic Leadership&Mobility: Sound judgment for ethical and business decision‑making, strong cross‑functional leadership acumen, and the ability to travel globally up to 30%.

Roche is an Equal Opportunity Employer. #J-18808-Ljbffr