Medical information Advisor

Location: Derio

Medical Information Advisor
Based remotely in Spain with up to 25% travel to Copenhagen, Denmark, and various international locations.

Department:
Clinical, Medical Safety and Surveillance (CMSS). Report to Senior Director of Medical Affairs.

In This Role, You Will Have The Opportunity To

Lead Medical Information Strategy: shape and execute the global medical information strategy, owning the development, quality, and lifecycle of scientific content and MAPSS assets while aligning cross‑functional stakeholders on strategic priorities.

Act as the Scientific and Clinical Expert: serve as a trusted subject‑matter expert in acute and emergency diagnostics, translating complex clinical evidence into clear, actionable insights that inform Medical Affairs, Marketing, and product development decisions.

Drive High‑Impact Scientific Communications: lead publication planning and execution, transforming clinical performance data into peer‑reviewed evidence and compelling medical materials that strengthen scientific credibility and support global adoption.

Build and Activate Global Expert Networks: develop and manage strategic relationships with KOLs and KEEs, leading engagement processes, supporting IIS initiatives, and enabling high‑value scientific collaborations that expand external impact.

Represent Medical Affairs Internally and Externally: play a visible role at scientific conferences and industry forums, delivering impactful presentations and ensuring consistent, compliant communication of medical insights across global stakeholders.

The Essential Requirements Of The Job Include

Advanced Credentials with Relevant Industry

Experience:

hold an advanced degree in Life Sciences (PhD, PharmD, MSc, or equivalent) combined with a minimum of 5 years of experience in Medical Affairs, Medical Information, or related roles within the IVD, medical device, pharma or healthcare industry, with strong exposure to clinical applications.

Strong Expertise in Medical Information and Processes: demonstrate in-depth knowledge of medical information tools, processes, and compliance requirements, with hands‑on experience developing, reviewing, and managing scientific and medical content in a regulated environment.

Exceptional Scientific Communication

Skills:

exhibit outstanding written and verbal communication in English, with proven ability to translate complex scientific data into clear, impactful messages for both expert and non‑expert audiences.

Solid Clinical and Technical Understanding: bring strong familiarity with IVD technologies and their application in clinical settings, particularly in acute or hospital‑based workflows, enabling meaningful scientific contribution and credible stakeholder engagement.

Effective Cross‑Functional Collaboration and Execution: show the ability to work effectively across Medical Affairs, Clinical, Marketing, and external stakeholders, managing multiple priorities while maintaining high standards of quality, compliance, and execution.

It would be a Plus if You Also Possess Previous Experience In

Technical/Scientific knowledge /experience in Clinical Chemistry.

Experience in Acute and Emergency care spaces.

Remote work arrangement is available for eligible roles, allowing you to work from home. Additional information will be provided during the interview process.

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