Medical Advisor


Düsseldorf
Permanent
Negotiable
Medical Affairs and HEOR
PR/547548_1748869626
Medical Advisor

EPM Scientific is partnering with a leading pharmaceutical company expanding its Medical Affairs function in Germany. This is a unique opportunity to shape medical strategy and drive scientific excellence in a dynamic, cross-functional environment.


Location: Germany (Remote/Hybrid options available)
Start Date: July/August 2025 (Flexible)
Contract Type: Permanent
Languages Required: Fluent in German and English
Therapeutic Area: Aesthetic Medicine

Key Responsibilities

  • Develop and execute medical strategies across the product lifecycle-from early development to post-launch.
  • Ensure alignment with global brand objectives and uphold scientific integrity.
  • Work closely with Marketing, Clinical Development, Regulatory Affairs, Patient Engagement, RWE, Legal, and Digital teams.
  • Integrate medical insights into strategic and operational planning.
  • Craft the medical narrative to guide evidence generation and communication.
  • Support publication planning, data dissemination, and scientific content development.
  • Clinical Research Oversight
  • Provide input and oversight for Phase IV trials, Investigator-Initiated Studies (IIS), and Early Access Programs (EAPs).
  • Organize and lead advisory boards, expert panels, and roundtables.
  • Represent the company at scientific congresses and patient engagement events.
  • Conduct medical landscape assessments, scenario planning, and competitive simulations to inform strategy.
  • Contribute to pharmacoeconomic value propositions and early access strategies for patients with unmet needs.
  • Support German medical teams in aligning with global strategies, including resource planning and launch readiness.
  • Collaborate with Key External Experts (KEEs) to gather insights that inform clinical development and brand strategy.


Candidate Profile

  • Proven experience in Medical Affairs within the pharmaceutical industry (Germany or EU).
  • Strong understanding of drug development, regulatory frameworks, and market access in Germany.
  • Expertise in clinical study design, data interpretation, and evidence generation.
  • Excellent communication and stakeholder management skills.
  • Ability to manage cross-functional projects independently.
  • Experience in competitive intelligence and strategic planning is a plus.

Interested?

If this opportunity aligns with your background and career goals, we encourage you to apply directly. If not, feel free to share it with someone in your network who might be a great fit.

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