LennTech Search
Medical Affairs Manager
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Medical Affairs Manager
Job Summary Drive scientific communication and evidence-support strategies to meet Commercial business needs. You will develop publications, abstracts, and presentations, conduct medical reviews of marketing claims, and manage the Investigator Initiated Studies (IIS) program. Serving as a subject matter expert, you will ensure all scientific outputs align with commercial priorities while maintaining strict regulatory and compliance standards.
Essential Functions & Accountabilities
Scientific Leadership & Claims Support Scientific Materials: Develop and review publications, conference abstracts, and presentations that translate commercial needs into compliant, robust communication materials. Program Oversight: Manage the IIS program to address strategic data gaps identified by Commercial, Clinical, and R&D. Medical Review (MLR/AdPromo): Review promotional and educational materials to ensure accuracy, balance, and compliance. Claims Substantiation: Provide scientific guidance on internal/external data and author technical memos or data-on-file documents to support commercial strategies.
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External & Cross-Functional Collaboration KOL Engagement: Support Commercial and Professional Affairs by providing scientific expertise for relationships with key opinion leaders and influencers. Defense & Inquiries: Formulate evidence-based responses to competitor challenges and handle off-label inquiries within compliant, non-promotional boundaries. Cross-Functional Input: Provide strategic medical/scientific insights to global brand and regional marketing teams to enable credible market execution.
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Experience & Education Industry Experience: 5+ years in Medical/Professional Affairs or related clinical/scientific roles (medical device industry strongly preferred). Clinical Experience: 5+ years of experience as an optometrist. Practice management experience is a plus. Education: Degree in Optometry (BOptom, MOptom, OD) or equivalent.
Knowledge, Skills & Abilities Strong proficiency in MLR/AdPromo processes and US/EU promotional regulations. Proven ability to interpret and communicate complex clinical data to legal, regulatory, commercial, and external audiences. Global market experience (multi-market exposure or additional language skills preferred). Exceptional organizational, written, and verbal communication skills. Proficiency in MS Office (Word, Excel, PowerPoint).
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