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Regional Medical Affairs Manager (ILD)(m/w/x)
Aligning cross-functional insights and providing structured feedback to global asset teams for ILD pipeline products. Advanced degree in Health Sciences and 5+ years Medical Affairs experience required. Home office, flexible working hours, and additional days off.
Requirements
- Advanced degree in Health Sciences (MD, PharmD, DVM)
- At least 5 years Medical Affairs experience
- Experience in multinational pharmaceutical company
- Respiratory TA experience is a strong asset
- Proven medical and scientific leadership
- Drive high-priority projects in collaboration
- Strong lateral leadership capabilities
- Excellent interpersonal, negotiation, communication skills
- Experience in a matrix environment
- Experience in CEE region is an asset
- Business-proficient English skills
- Willingness to travel frequently
- Availability to travel frequently
Tasks
- Identify country-specific stakeholder needs and market specifics
- Analyze impact on pipeline products
- Align insights cross-functionally
- Provide structured feedback to global asset teams
- Build and maintain scientific and medical expertise
- Contribute to design and approval of regional materials
- Ensure compliance with global standards, legal regulations, and internal SOPs
- Support successful regional launch of new products and indications
- Implement publication strategies aligned with global and ROPU product positioning
- Co-create and execute the RCV Integrated Customer Plan (ICP)
- Engage cross-functional stakeholders for aligned medical activities
- Lead mapping of regional and local patient journeys
- Identify gaps in diagnostics and disease management
- Engage external experts, healthcare professionals, and patient advocacy representatives
- Gather insights on product and data needs
- Plan and initiate Real World Data generation and collection
- Conduct non-interventional studies and non-trial activities
- Collect ECRs
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
- Vegetarian and vegan options
Learning & Development
- Diverse training and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
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Regional Medical Affairs Manager (ILD)(m/w/x)
Aligning cross-functional insights and providing structured feedback to global asset teams for ILD pipeline products. Advanced degree in Health Sciences and 5+ years Medical Affairs experience required. Home office, flexible working hours, and additional days off.
Requirements
- Advanced degree in Health Sciences (MD, PharmD, DVM)
- At least 5 years Medical Affairs experience
- Experience in multinational pharmaceutical company
- Respiratory TA experience is a strong asset
- Proven medical and scientific leadership
- Drive high-priority projects in collaboration
- Strong lateral leadership capabilities
- Excellent interpersonal, negotiation, communication skills
- Experience in a matrix environment
- Experience in CEE region is an asset
- Business-proficient English skills
- Willingness to travel frequently
- Availability to travel frequently
Tasks
- Identify country-specific stakeholder needs and market specifics
- Analyze impact on pipeline products
- Align insights cross-functionally
- Provide structured feedback to global asset teams
- Build and maintain scientific and medical expertise
- Contribute to design and approval of regional materials
- Ensure compliance with global standards, legal regulations, and internal SOPs
- Support successful regional launch of new products and indications
- Implement publication strategies aligned with global and ROPU product positioning
- Co-create and execute the RCV Integrated Customer Plan (ICP)
- Engage cross-functional stakeholders for aligned medical activities
- Lead mapping of regional and local patient journeys
- Identify gaps in diagnostics and disease management
- Engage external experts, healthcare professionals, and patient advocacy representatives
- Gather insights on product and data needs
- Plan and initiate Real World Data generation and collection
- Conduct non-interventional studies and non-trial activities
- Collect ECRs
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
- Vegetarian and vegan options
Learning & Development
- Diverse training and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
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