About The Position
The Manager Global Scientific Affairs will support the development and execution of scientific communications and medical activities for assigned assets. The role will work closely with the Global Scientific Affairs and Medical Affairs leads to ensure high-quality delivery of congress materials, medical education and training initiatives, while enabling efficient cross-functional collaboration. The role focuses on operational execution, project coordination, and content support, ensuring timely and compliant implementation of scientific strategies.
Requirements
- Advanced degree (PhD, PharmD) or MSc in life sciences (PhD preferred but can be flexible depending on seniority)
- 2–5 years’ experience in Medical Affairs, Scientific Communications, or pharma/biotech
- Experience in working and collaborating with Market Access, Medical Affairs, Clinical, Legal, Regulatory and Compliance
- Role model with the highest scientific and ethical standards, working in accordance with applicable rules and regulations
- Outstanding communication skills, both written and oral
- Strategic thinking, Prioritisation and time management skills and strong sense of accountability
- Proficiency in Microsoft Windows, Word, Excel, and PowerPoint required
- Fluency in English
Nice To Haves
- Experience in Cardiometabolic disorders is preferred
- Collaborative team player with interpersonal skills, able to work effectively in a team setting and interact respectfully with people of different cultural, seniority and functional backgrounds
- other European languages a bonus
Responsibilities
- Assist in drafting, reviewing, and formatting scientific materials
- Maintain trackers and ensure milestone adherence
- Coordinate congress deliverables
- Liaise with internal stakeholders and agencies for content development
- Ensure alignment of materials with scientific and compliance requirement
- Support development and rollout of internal and external training materials
- Coordinate logistics for training activities (content, speakers, timelines)
- Maintain training materials repository and updates
- Act as a key operational interface with: Medical Affairs, Regulatory & Compliance, Clinical and Market Access, Affiliate medical teams
- Track deliverables and ensure alignment across stakeholders
- Prepare internal updates, slide decks, and reporting materials
- Maintain project plans, trackers, and communication timelines
- Identify risks or delays and proactively escalate
- Support implementation of digital/multichannel initiatives
- Ensure documentation is compliant and audit-ready
- Conduct literature searches and summarize key scientific insights
- Monitor external developments relevant to assigned assets
- Support preparation of internal scientific briefings
- Support the scientific communications strategy for assigned assets
- Work with the cross-functional teams and external agencies to define appropriate medical communication solutions to support product/disease area strategy implementation across geographies
- Support, develop and execute key training needs of the affiliates
- Support the development efforts for external medical education and training
- Contribute to innovative digital/multichannel approaches for the dissemination of medical materials
- Stay abreast of internal and external developments relevant to the assigned assets
Benefits
- Competitive compensation for your work
- Emphasis on work/life balance
- Collaborative and team-oriented environment
- Opportunities for professional growth
- Diversity and Inclusion
- Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
