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Director, Global Medical Affairs - Publications(m/w/x)
Developing scientific publications and presentations for targeted radiopharmaceuticals in oncology. 7-10 years of publication leadership in biotech/pharma required. Flexible hours, home office options, and special payments.
Requirements
- Advanced degree (MD, PharmD, or PhD) in Oncology, Nuclear Medicine, or related scientific discipline
- 7-10 years leading publications in Medical Affairs, preferably oncology, radiopharmaceuticals, or specialty therapeutics
- Extensive publication management, medical writing, and clinical trial publications experience in biotech or pharmaceutical industry
- In-depth knowledge of GCP, ICH guidelines, medical compliance, and scientific dissemination strategies
- Strong project management and organizational skills for multiple concurrent publications, priorities, and deadlines
- Effective collaboration in cross-functional and matrixed organizations with stakeholders, experts, and KOLs
- Exceptional scientific writing, editing, communication, and presentation skills; strong English proficiency
Tasks
- Lead annual publication plan development
- Execute and optimize publication strategies
- Develop scientific publications
- Create abstracts, posters, and oral presentations
- Submit manuscripts to peer-reviewed journals
- Coordinate internal publication review
- Manage external publication approval
- Collaborate with Clinical Research, Biostatistics, Regulatory Affairs, Dosimetry, and Global Medical Affairs
- Ensure scientific accuracy
- Maintain regulatory compliance
- Adhere to FDA regulations, ICH guidelines, and journal requirements
- Oversee disclosure management
- Manage conflict of interest documentation
- Conduct quality reviews of publication materials
- Manage journal submission workflows
- Track publication timelines
- Coordinate with external investigators, agencies, and scientific conferences
- Oversee budgets and timelines
- Manage vendors
- Adapt publication strategies to emerging clinical data
- Adjust strategies based on trial milestones and regulatory updates
Work Experience
- 7 - 10 years
Education
- Master's degree
Languages
- English – Native
Benefits
Flexible Working
- Flexible working hours
- Home office options
Learning & Development
- Comprehensive onboarding programme
- Individually tailored further training programme
- German courses
- English courses
Bonuses & Incentives
- Attractive special payments
Competitive Pay
- Employee participation programme
Company Bike
- Job bike
Public Transport Subsidies
- Subsidised job ticket
Retirement Plans
- Above-average contribution to company pension scheme
Healthcare & Fitness
- Health promotion programmes
- EGYM Wellpass
- Subsidy for local fitness studio
Social Impact
- Sponsorship of sporting events
Mentorship & Coaching
- Lifestyle coaching sessions
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Director, Global Medical Affairs - Publications(m/w/x)
Developing scientific publications and presentations for targeted radiopharmaceuticals in oncology. 7-10 years of publication leadership in biotech/pharma required. Flexible hours, home office options, and special payments.
Requirements
- Advanced degree (MD, PharmD, or PhD) in Oncology, Nuclear Medicine, or related scientific discipline
- 7-10 years leading publications in Medical Affairs, preferably oncology, radiopharmaceuticals, or specialty therapeutics
- Extensive publication management, medical writing, and clinical trial publications experience in biotech or pharmaceutical industry
- In-depth knowledge of GCP, ICH guidelines, medical compliance, and scientific dissemination strategies
- Strong project management and organizational skills for multiple concurrent publications, priorities, and deadlines
- Effective collaboration in cross-functional and matrixed organizations with stakeholders, experts, and KOLs
- Exceptional scientific writing, editing, communication, and presentation skills; strong English proficiency
Tasks
- Lead annual publication plan development
- Execute and optimize publication strategies
- Develop scientific publications
- Create abstracts, posters, and oral presentations
- Submit manuscripts to peer-reviewed journals
- Coordinate internal publication review
- Manage external publication approval
- Collaborate with Clinical Research, Biostatistics, Regulatory Affairs, Dosimetry, and Global Medical Affairs
- Ensure scientific accuracy
- Maintain regulatory compliance
- Adhere to FDA regulations, ICH guidelines, and journal requirements
- Oversee disclosure management
- Manage conflict of interest documentation
- Conduct quality reviews of publication materials
- Manage journal submission workflows
- Track publication timelines
- Coordinate with external investigators, agencies, and scientific conferences
- Oversee budgets and timelines
- Manage vendors
- Adapt publication strategies to emerging clinical data
- Adjust strategies based on trial milestones and regulatory updates
Work Experience
- 7 - 10 years
Education
- Master's degree
Languages
- English – Native
Benefits
Flexible Working
- Flexible working hours
- Home office options
Learning & Development
- Comprehensive onboarding programme
- Individually tailored further training programme
- German courses
- English courses
Bonuses & Incentives
- Attractive special payments
Competitive Pay
- Employee participation programme
Company Bike
- Job bike
Public Transport Subsidies
- Subsidised job ticket
Retirement Plans
- Above-average contribution to company pension scheme
Healthcare & Fitness
- Health promotion programmes
- EGYM Wellpass
- Subsidy for local fitness studio
Social Impact
- Sponsorship of sporting events
Mentorship & Coaching
- Lifestyle coaching sessions
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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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