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Medical Affairs Manager - Publications(m/w/x)
Leading scientific content development for targeted radiopharmaceuticals in a biotech group. Advanced degree (MD, PharmD, or PhD) in oncology/nuclear medicine and 3+ years medical writing experience in biotech/pharma required. Employee participation program, job bike.
Requirements
- Advanced degree (MD, PharmD, or PhD) in oncology, nuclear medicine, or related scientific discipline
- Minimum 3+ years medical writing experience, ideally within Medical Affairs, preferably in oncology, radiopharmaceuticals, or specialty therapeutics
- Proven experience in publication management and clinical trial publications within biotech or pharma
- Strong track record of cross-functional collaboration in matrixed organizations
- Deep understanding of GCP, ICH, and medical compliance standards
- Exceptional scientific writing and editing skills with strong attention to detail and quality focus
- Solid project management abilities with capacity to manage multiple concurrent publications and deadlines
- Business fluent German and English
Tasks
- Lead development of abstracts, posters, presentations, and manuscripts.
- Coordinate and manage internal and external publication reviews.
- Drive cross-functional collaboration for impactful publications.
- Ensure scientific accuracy.
- Ensure regulatory compliance (FDA, ICH, GCP).
- Ensure adherence to journal and ethical guidelines.
- Oversee disclosure management.
- Oversee conflict of interest documentation.
- Oversee quality control of publication materials.
- Develop and execute the annual publication plan.
- Align publication plan with strategic priorities and objectives.
- Align publication plan with timelines and pipeline milestones.
- Manage publication tracking systems.
- Manage journal submissions.
- Manage conference communications.
- Manage publication budgets.
- Manage vendors and external partners.
- Support internal and external education initiatives.
- Incorporate emerging clinical data into publication strategies.
- Incorporate regulatory updates into publication strategies.
Work Experience
- 3 years
Education
- Doctoral / PhD
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GCP
- ICH
Benefits
Flexible Working
- Flexible working hours
- Home office options
Bonuses & Incentives
- Attractive special payments
Competitive Pay
- Employee participation programme
Company Bike
- Job bike
Public Transport Subsidies
- Subsidised job ticket
Retirement Plans
- Above-average company pension contribution
Learning & Development
- Individually tailored further training programme
- German courses
- English courses
Healthcare & Fitness
- Health promotion programmes
- EGYM Wellpass
- Subsidy for local fitness studio
Team Events
- Sponsorship of sporting events
Mentorship & Coaching
- Lifestyle coaching sessions
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Medical Affairs Manager - Publications(m/w/x)
Leading scientific content development for targeted radiopharmaceuticals in a biotech group. Advanced degree (MD, PharmD, or PhD) in oncology/nuclear medicine and 3+ years medical writing experience in biotech/pharma required. Employee participation program, job bike.
Requirements
- Advanced degree (MD, PharmD, or PhD) in oncology, nuclear medicine, or related scientific discipline
- Minimum 3+ years medical writing experience, ideally within Medical Affairs, preferably in oncology, radiopharmaceuticals, or specialty therapeutics
- Proven experience in publication management and clinical trial publications within biotech or pharma
- Strong track record of cross-functional collaboration in matrixed organizations
- Deep understanding of GCP, ICH, and medical compliance standards
- Exceptional scientific writing and editing skills with strong attention to detail and quality focus
- Solid project management abilities with capacity to manage multiple concurrent publications and deadlines
- Business fluent German and English
Tasks
- Lead development of abstracts, posters, presentations, and manuscripts.
- Coordinate and manage internal and external publication reviews.
- Drive cross-functional collaboration for impactful publications.
- Ensure scientific accuracy.
- Ensure regulatory compliance (FDA, ICH, GCP).
- Ensure adherence to journal and ethical guidelines.
- Oversee disclosure management.
- Oversee conflict of interest documentation.
- Oversee quality control of publication materials.
- Develop and execute the annual publication plan.
- Align publication plan with strategic priorities and objectives.
- Align publication plan with timelines and pipeline milestones.
- Manage publication tracking systems.
- Manage journal submissions.
- Manage conference communications.
- Manage publication budgets.
- Manage vendors and external partners.
- Support internal and external education initiatives.
- Incorporate emerging clinical data into publication strategies.
- Incorporate regulatory updates into publication strategies.
Work Experience
- 3 years
Education
- Doctoral / PhD
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GCP
- ICH
Benefits
Flexible Working
- Flexible working hours
- Home office options
Bonuses & Incentives
- Attractive special payments
Competitive Pay
- Employee participation programme
Company Bike
- Job bike
Public Transport Subsidies
- Subsidised job ticket
Retirement Plans
- Above-average company pension contribution
Learning & Development
- Individually tailored further training programme
- German courses
- English courses
Healthcare & Fitness
- Health promotion programmes
- EGYM Wellpass
- Subsidy for local fitness studio
Team Events
- Sponsorship of sporting events
Mentorship & Coaching
- Lifestyle coaching sessions
About the Company
ITM Isotope Technologies Munich SE
Industry
Pharmaceuticals
Description
Das Unternehmen entwickelt, produziert und vertreibt zielgerichtete diagnostische und therapeutische Radiopharmazeutika sowie Radioisotope für die Krebsbehandlung.
Not a perfect match?
- ITM Isotope Technologies Munich SE
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Senior Manager, Medical Communication(m/w/x)
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Senior Medical Lead - New Launches(m/w/x)
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