Immunic AG
Medical Director(m/w/x)
Full-timeOn-siteExperienced
Gräfelfing
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Driving Phase 3 protocol development and regulatory interactions for immunology therapies. MD with 3-5+ years clinical trial experience in Progressive MS essential. Stock option program participation, Wellpass.
Requirements
- Medical Degree (MD), ideally with training or clinical background in neurology
- 3-5+ years experience in biotech/pharma or academic clinical research, preferably with direct involvement in clinical trials in Progressive MS
- Strong expertise in Multiple Sclerosis, 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 assessing risks, opportunities, and implications in late-stage drug development
- Effective leadership and collaboration in cross-functional and matrix team structures
- Excellent communication skills and strategic mindset
- Native-level English proficiency
Tasks
- Lead study planning and execution.
- Define key medical strategies.
- Drive Phase 3 protocol development.
- Execute medical strategy for Phase 3 trials.
- Lead regulatory interactions (e.g., FDA/EMA).
- Oversee ongoing patient safety monitoring.
- Review serious adverse events (SAEs).
- Collaborate with external medical experts.
- Ensure scientific excellence and study delivery.
- Collaborate with medical advisory board and investigators.
- Represent the study at scientific meetings.
- Collaborate with cross-functional teams.
- Align on study milestones.
- Align on data readouts.
- Align on launch preparation.
- Analyze and interpret Phase 3 data.
- Support regulatory submissions, reimbursement, and scientific publications.
Work Experience
- 3 - 5 years
Education
- Bachelor's degree
Languages
- English – Native
Tools & Technologies
- Good Clinical Practice (GCP)
Benefits
Career Advancement
- Professional growth opportunities
Informal Culture
- International and highly motivated team
Startup Environment
- Dynamic, flexible, and innovative work environment
Competitive Pay
- Stock option program participation
Healthcare & Fitness
- Wellpass
Mental Health Support
- OpenUp
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immunic AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Driving Phase 3 protocol development and regulatory interactions for immunology therapies. MD with 3-5+ years clinical trial experience in Progressive MS essential. Stock option program participation, Wellpass.
Requirements
- Medical Degree (MD), ideally with training or clinical background in neurology
- 3-5+ years experience in biotech/pharma or academic clinical research, preferably with direct involvement in clinical trials in Progressive MS
- Strong expertise in Multiple Sclerosis, 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 assessing risks, opportunities, and implications in late-stage drug development
- Effective leadership and collaboration in cross-functional and matrix team structures
- Excellent communication skills and strategic mindset
- Native-level English proficiency
Tasks
- Lead study planning and execution.
- Define key medical strategies.
- Drive Phase 3 protocol development.
- Execute medical strategy for Phase 3 trials.
- Lead regulatory interactions (e.g., FDA/EMA).
- Oversee ongoing patient safety monitoring.
- Review serious adverse events (SAEs).
- Collaborate with external medical experts.
- Ensure scientific excellence and study delivery.
- Collaborate with medical advisory board and investigators.
- Represent the study at scientific meetings.
- Collaborate with cross-functional teams.
- Align on study milestones.
- Align on data readouts.
- Align on launch preparation.
- Analyze and interpret Phase 3 data.
- Support regulatory submissions, reimbursement, and scientific publications.
Work Experience
- 3 - 5 years
Education
- Bachelor's degree
Languages
- English – Native
Tools & Technologies
- Good Clinical Practice (GCP)
Benefits
Career Advancement
- Professional growth opportunities
Informal Culture
- International and highly motivated team
Startup Environment
- Dynamic, flexible, and innovative work environment
Competitive Pay
- Stock option program participation
Healthcare & Fitness
- Wellpass
Mental Health Support
- OpenUp
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immunic AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Immunic AG
Industry
Pharmaceuticals
Description
Immunic Therapeutics is a biotechnology company developing immunology therapies for chronic inflammatory and autoimmune diseases.
Not a perfect match?
- Immunic AG
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