Senior Medical Director (m/f/x)

Your mission

We are looking for a hands-on Senior Medical Director (m/f/x) to support our global Phase 3 registrational study in progressive Multiple Sclerosis. In this role, you will provide medical and clinical leadership across study planning and execution, define key medical strategies, and drive protocol development. You will serve as the clinical representative in regulatory interactions, oversee ongoing safety monitoring, and collaborate closely with external medical experts to ensure scientific excellence and successful study delivery.

• Clinical Strategy & Leadership: Define and execute the medical strategy for Phase 3 clinical trials, including protocol design, study execution, and data analysis. 
• Regulatory & Safety Oversight: Provide medical leadership during regulatory interactions (e.g., FDA/EMA) and oversee patient safety, including review of serious adverse events (SAEs). 
• Scientific Expertise & External Engagement: Act as the primary medical expert, collaborating with the medical advisory board and investigators, and representing the study at scientific meetings. 
• Cross-Functional Collaboration: Work closely with Clinical Operations, Regulatory Affairs, Medical Affairs, and Commercial teams to align on study milestones, data readouts, and launch preparation. 
• Data Interpretation: Analyze and interpret Phase 3 data to support regulatory submissions, reimbursement activities, and scientific publications.

Your profile

• Medical Degree (MD), ideally with training or clinical background in neurology.
• 3-5+ years of experience in biotech or pharma industry or in academic clinical research, preferably with direct involvement in clinical trials in Progressive MS. 
• Strong expertise in Multiple Sclerosis, with deep scientific understanding of disease mechanisms and clinical development pathways.
• Solid knowledge of Good Clinical Practice (GCP) and international regulatory requirements (FDA, EMA).
• Experience in assesing risks, opportunities, and implications in late-stage drug development. 
• Ability to lead and collaborate effectively in cross-functional and matrix team structures.
• Excellent communication skills and a strategic mindset. 
• Native-level English proficiency.

Why us?

We offer 

• A permanent position in an international and highly motivated team.
• A dynamic, flexible and innovative working environment.
• Participation in our company’s success through our stock option program.
• Competitive compensation, comprehensive benefits and opportunities for professional growth.
• Further benefits that promote our employee’s health and well-being: Wellpass, OpenUp, and more.

 
Join us and be part of a company where your work directly contributes to our mission of improving
patient care through groundbreaking research. Immunic AG offers a stimulating work environment where
innovation and collaboration are valued.