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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in building relationships with healthcare professionals and stakeholders while effectively communicating scientific data. Proficient in supporting clinical trials and ensuring compliance with industry regulations.
Highest-signal resume keywords
MD Or Master's Degree In Life SciencesPrevious Experience As An MSLStrong Ability To Interpret Scientific DataFluency In Danish And EnglishExperience Engaging With Healthcare Professionals
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
PhD Or Equivalent Scientific QualificationClinical Trial Feasibility AssessmentEvidence Generation ActivitiesProduct Launch PreparationLifecycle Management Activities
Soft Skills
Excellent Communication SkillsRelationship-Building SkillsStrong Influencing CapabilitiesCollaborative MindsetScientific Curiosity
Industry Keywords
Medical AffairsPharmaceutical IndustryStakeholder ManagementNordic RegionCompliance Requirements
About the role
Key responsibilities & impact- Build and maintain trusted relationships with healthcare professionals, researchers, professional associations, and key external experts
- Serve as the primary scientific point of contact for healthcare professionals and external stakeholders
- Conduct scientific exchanges and provide timely, accurate responses to medical information requests
- Lead and support advisory boards, scientific meetings, congresses, and educational initiatives
- Develop and execute engagement plans for key external experts and support speaker development activities
- Gather, analyze, and communicate medical insights from the field to inform strategic decision making
- Support clinical trial feasibility assessments, investigator-initiated studies, and evidence generation activities
- Maintain up-to-date knowledge of assigned therapeutic areas, pipeline developments, and competitive landscape
- Collaborate with Medical Affairs, Commercial, Market Access, Clinical Development, and other teams
- Contribute to product launch preparation and lifecycle management activities across the Nordic region
- Ensure activities comply with company policies, compliance requirements, and applicable regulations
- Approximately 80% customer-facing activity
- Report directly to the Head of Medical Affairs Nordics
Requirements
What you’ll need- MD, or Master's degree in Life Sciences, Pharmacy, or a related field combined with a PhD or equivalent scientific qualification
- Previous experience as an MSL, Medical Advisor, Clinical Scientist, or related Medical Affairs role
- Strong ability to interpret, analyze, and communicate scientific and clinical data
- Experience engaging with healthcare professionals and scientific stakeholders
- Pharmaceutical industry and/or clinical experience highly desirable
- Excellent communication, presentation, and relationship-building skills
- Strong influencing and stakeholder management capabilities
- Collaborative mindset and ability to work independently
- Scientific curiosity, learning agility, and passion for medical dialogue
- Fluency in Danish and English
- Additional Nordic language skills considered an advantage
Benefits
Comp & perks- Excellent development opportunities within a global biopharmaceutical company
- Broad cross-functional and international collaboration
- Purpose-driven culture focused on improving patients' lives
- Inclusion and belonging culture
- Equal opportunity employer
- Reasonable accommodation available for applicants with disabilities