Global Medical Affairs Senior Manager

Silimed

22h•Remote

About The Position

The Global Medical Affairs Senior Manager supports the development and execution of global Medical Affairs strategies and scientific initiatives aligned with corporate objectives and regional needs. The role builds strategic scientific partnerships with Key Opinion Leaders, investigators, and healthcare stakeholders; leads balanced, evidence-based scientific exchange; and gathers medical insights to inform strategy, product lifecycle management, and evidence generation. The position provides scientific leadership across the product lifecycle, supports evidence-generation initiatives such as investigator-initiated studies, real-world evidence, publications, and scientific collaborations, and reviews scientific and promotional materials for accuracy, regulatory compliance, and consistency with approved product labeling. It works closely with Clinical Affairs, Regulatory Affairs, Quality, Marketing, Market Access, and Commercial teams while preserving Medical Affairs independence and scientific integrity. The role also contributes to advisory boards, congresses, expert meetings, publication strategies, and compliant medical communications. This is a full remote position within one of the company’s European headquarters locations: Austria, Belgium, Germany, Denmark, Netherlands, Spain, Italy, Turkey, or the UK.

Requirements

Bachelor's degree in Life Sciences, Pharmacy, Medicine, Biomedical Sciences, or a related healthcare discipline.
At least 10 years of experience in the pharmaceutical, biotechnology, or medical device industry.
If lacking previous experience in breast implants, a PhD or master’s in healthcare is mandatory.
Fluent English.
Strong scientific acumen and ability to critically evaluate, interpret, and communicate clinical evidence.
Excellent scientific communication skills for internal and external stakeholders.
Ability to develop and maintain trusted scientific partnerships with KOLs, investigators, and healthcare professionals.
Expertise in KOL engagement, medical insight generation, and translating field insights into actionable medical strategies.
Strong understanding of Medical Affairs principles, scientific exchange, evidence generation, and product lifecycle management.
Experience reviewing scientific claims and promotional materials for scientific accuracy, regulatory compliance, and alignment with approved labeling.
Strategic thinking and ability to identify evidence gaps, emerging clinical trends, and opportunities.
Cross-functional collaboration skills, including the ability to influence without authority while maintaining Medical Affairs independence.
Strong project management and organizational skills, including prioritizing multiple initiatives in a fast-paced global environment.
High ethical standards, sound scientific judgment, and commitment to regulatory and industry-code compliance.
Adaptability in multicultural, cross-regional, and matrix organizations.

Nice To Haves

Experience in breast implants.
Previous exposure to Medical Affairs, Medical Education, scientific projects, or healthcare stakeholder engagement.
Fluent Spanish.
Basic Portuguese.

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 other healthcare stakeholders.
Lead balanced, evidence-based scientific exchange with external experts.
Identify evidence gaps and support investigator-initiated studies, real-world evidence initiatives, clinical publications, and scientific collaborations.
Gather, analyze, and communicate medical insights from healthcare professionals, KOLs, and international markets to inform medical strategy, product lifecycle management, and evidence-generation activities.
Provide scientific leadership and medical support throughout the product lifecycle, including evidence dissemination, scientific communications, and responses to medical information requests.
Review and approve scientific and promotional claims, marketing materials, educational content, and external communications for scientific accuracy, clinical relevance, regulatory compliance, and consistency with approved labeling.
Partner with Clinical Affairs, Regulatory Affairs, Quality, Marketing, Market Access, and Commercial teams while maintaining Medical Affairs independence and scientific integrity.
Contribute to planning and execution of advisory boards, scientific congresses, expert meetings, and publication strategies.
Support the development, review, and approval of scientific publications, abstracts, manuscripts, medical presentations, and evidence summaries.
Monitor scientific literature, clinical evidence, treatment guidelines, competitor activities, and healthcare trends to identify opportunities and support medical planning.
Ensure Medical Affairs activities comply with applicable regulations, ethical standards, industry codes of practice, and company policies.