Global Medical Affairs Senior Manager

New
S
SilimedMedical devices
Full remote position wihtin one of our HQ in Europe. (Austria, Belgium, Germany, Portugal, Sweden, Denmark, Netherlands, Spain, Italy, Turkey, UK)ContractManager
Salary not disclosed
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Job Details

Languages
Fluent English is required. Fluent Spanish and basic Portuguese are highly desirable and would be considered an asset.
Experience
Minimum 10 years of experience within the pharmaceutical, biotechnology, or medical device industry.
Required Skills
Project Management

Requirements

  • Hold a bachelor's degree in Life Sciences, Pharmacy, Medicine, Biomedical Sciences, or a related healthcare discipline.
  • Have a PhD or master’s in healthcare if you do not have previous experience in breast implants.
  • Have a minimum of 10 years of experience in the pharmaceutical, biotechnology, or medical device industry.
  • Bring experience in Medical Affairs, Medical Education, scientific projects, or healthcare stakeholder engagement; this is preferred.
  • Demonstrate strong scientific acumen and the ability to evaluate, interpret, and communicate clinical evidence.
  • Have expertise in KOL engagement, medical insight generation, and translating field insights into medical strategies.
  • Understand Medical Affairs principles, scientific exchange, evidence generation, and product lifecycle management.
  • Be experienced in reviewing scientific claims and promotional materials for accuracy, regulatory compliance, and alignment with approved labeling.
  • Demonstrate project management and organizational skills, including the ability to prioritize multiple initiatives.
  • Meet high ethical standards and comply with industry regulations and codes of practice.
  • Be fluent in English.
  • Fluent Spanish and basic Portuguese are desirable assets.

Responsibilities

  • Support the development and execution of global Medical Affairs strategies and scientific initiatives aligned with corporate objectives and regional needs.
  • Develop and maintain scientific partnerships with Key Opinion Leaders, investigators, and healthcare stakeholders.
  • Lead balanced, evidence-based scientific exchange with external experts.
  • Identify evidence gaps and support investigator-initiated studies, real-world evidence, clinical publications, and scientific collaborations.
  • Gather, analyze, and communicate medical insights from healthcare professionals, KOLs, and international markets.
  • Provide scientific leadership throughout the product lifecycle, including evidence dissemination, scientific communications, and medical information responses.
  • Review and approve scientific and promotional claims, marketing materials, educational content, and external communications for accuracy and compliance.
  • Partner with Clinical Affairs, Regulatory Affairs, Quality, Marketing, Market Access, and Commercial teams while maintaining Medical Affairs independence.
  • Contribute to advisory boards, scientific congresses, expert meetings, and publication strategies.
  • Monitor scientific literature, clinical evidence, treatment guidelines, competitor activities, and healthcare trends.
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