Medical Scientific Advisor – Gyn, GU, GI

AstraZeneca

. Develop and execute the country scientific engagement plan .

Posted 11/11/2026full-timeCopenhagen • DenmarkMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in scientific engagement and stakeholder collaboration, with a strong focus on evidence generation, clinical trials, and market access strategies. Proficient in scientific communication and compliance within the pharmaceutical industry.

Highest-signal resume keywords

Advanced Life-Sciences DegreeScientific Stakeholder EngagementClinical Trials ExperiencePharmaceutical Medical AffairsEvidence Generation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Evidence SynthesisScientific CommunicationInsight GenerationClinical Trial FeasibilityRegulatory Submissions

Soft Skills

Cross-Functional CollaborationInfluencing SkillsRelationship Building

Tools & Technologies

Digital ToolsAI-Enabled ToolsAnalytics PlatformsManagement Systems

Certifications & Qualifications

Valid Driver's LicenseLocal Material Certification

Industry Keywords

Medical AffairsReal-World EvidenceHTA SubmissionsPharmacovigilanceEthical Standards

About the role

Key responsibilities & impact

Develop and execute the country scientific engagement plan
Build trusted relationships with experts, societies, investigators and healthcare stakeholders
Lead balanced, non-promotional scientific dialogue
Respond compliantly to unsolicited requests
Manage advisory boards in line with procedures
Identify pathway bottlenecks, diagnostic gaps and adoption barriers
Translate insights into recommendations for strategy, evidence generation, launches and access
Support launch readiness, medical education, scientific narrative development, objection handling and healthcare-system initiatives
Identify local evidence gaps and support real-world evidence and externally sponsored research
Contribute to clinical-trial feasibility, site engagement and delivery
Provide scientific input to HTA, formulary and protocol submissions, guidelines and appropriate-use initiatives
Ensure compliance with local codes, SOPs and ethical standards
Support medical review, pharmacovigilance and inspection readiness
Act as a therapy-area subject-matter expert
Deliver scientific training and collaborate with cross-functional and Nordic teams

Requirements

What you’ll need

Advanced life-sciences degree, such as MSc, PharmD, MD or PhD
Proven deliverables in the relevant therapy area and scientific stakeholder engagement
Strong ability to generate insights, synthesize evidence and translate findings into action
Understanding of clinical trials, evidence generation and medical support for market access
Excellent scientific communication, influencing and cross-functional collaboration skills
Ability to use digital and AI-enabled tools with scientific rigor, compliance and sound judgment
Valid driver’s license for this field-based position
Fluency in the local language and English
PhD, MD, MBA or other relevant advanced qualifications desirable
Pharmaceutical Medical Affairs experience, particularly in pre-launch or launch environments, desirable
Experience in clinical trials, RWE or externally sponsored research desirable
Experience supporting HTA, formulary or protocol submissions desirable
Eligibility for local material certification desirable
Proficiency with analytics, insight platforms and relevant management systems desirable

Benefits

Comp & perks

Performance-aligned reward approach supporting commercial growth, scientific advancement, collaboration and personal development
Flexible benefits offering where possible
Rewards recognizing contributions and unique insights
Inclusive and diverse workplace culture
Opportunities for personal development, learning and growth
Support for bold ideas, ambition and innovation