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Galderma

Associate Director, Medical Strategic Operations

Galderma, Boston, Massachusetts, us, 02298

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Associate Director, Medical Strategic Operations

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Associate Director, Medical Strategic Operations

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Galderma Associate Director, Medical Strategic Operations

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Associate Director, Medical Strategic Operations

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Galderma Get AI-powered advice on this job and more exclusive features. At Galderma we're unique and we embrace difference. Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make - working here isn't like anywhere else. At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Based at our Boston Offive, the

Associate Director, Medical Strategic Operations

will lead the strategic execution of the Nemolizumab US Medical Affairs (USMA) brand plan and drive operational excellence across both headquarters and field medical teams. This role is responsible for ensuring effective implementation of medical tactics in alignment with strategic objectives, budget phasing, and compliance requirements. Working closely with the Head of USMA for Nemolizumab and cross-functional partners, the Associate Director will manage key initiatives including strategic planning, project and budget management, dashboard development, and vendor operations. This position plays a critical role in supporting the successful delivery of medical programs that advance the scientific understanding of Nemolizumab in the US. Essential Functions Collaborate with the Head of US Medical Affairs (USMA) Nemolizumab to lead the development, tracking, and execution of the overall US Medical strategic and tactical plan. Partner with USMA strategic, field Medical Leadership and cross-functional teams to track tactical plans with strategic objectives, financial milestones and ensure timeline-oriented execution. Develop high-quality presentation materials (e.g., slide decks) to support strategic discussions, leadership updates, cross-functional alignment, and long-range planning initiatives. Must be able to synthesize complex information into clear, compelling visuals and narratives. Lead the development and maintenance of USMA Nemolizumab dashboards to track tactical execution, KPIs/metrics, insights; synthesize findings into insights and recommendations for decision making and strategic planning. Partner closely with finance and FP&A teams to develop, track, and manage the US Medical Affairs budget, ensuring spend aligns with phasing and forecast. Manage and oversee all vendor (including HCPs) and contract operations, including securing MSAs, SOWs, opening POs, and ensuring timely execution to support team. Provide leadership on project management support for all US Medical Affairs-led programs, ensuring alignment with tactical objectives, KPIs and timelines. Maintain a robust congress calendar with assigning accountabilities to internal USMA nemo medical stakeholders for congresses. Lead and support medical leadership meetings and forums by developing meeting agendas, creating slide decks, tracking action items, and driving accountability across stakeholders. Support compliance review and approval processes for regional and national advisory boards, ensuring adherence to legal and regulatory requirements. Coordinate submission and approval of field medical materials through the Medical Review Board (MRB), including field resources, advisory board content, and congress materials. Support onboarding of new personnel, through creating custom onboarding plans in coordination with team members Improve and implement new procedures to streamline medical operations (home office and field), ensuring compliance with regulatory and company guidelines. Support creation of quantitative insight reports using Veeva and Power BI in partnership with the National MSL Director to capture and communicate field metrics. Support additional operational or project management activities as needed. Minimum Education, Knowledge, Skills, and Abilities Advanced degree

(PharmD, PhD, MD) with

1-3+ years

of experience in medical affairs or life sciences consulting OR Master's degree

(M.S.) in a related field with

5+ years

of experience in medical affairs strategy/operations or commercial operational excellence, including strategic planning and operational/project management OR Bachelor's degree

in healthcare or life sciences with

7+ years

of experience in medical affairs strategy/operations or commercial operational excellence, including strategic planning and operational/project management. Proven ability to create professional, visually compelling slide decks and presentation materials for leadership and cross-functional teams; proficiency in PowerPoint (or equivalent tools) required. Strong experience developing and managing dashboards to track KPIs, tactical progress, and insights; proficiency in tools such as Power BI, Excel, or other visualization platforms preferred. Demonstrated experience managing budgets in collaboration with Finance and FP&A teams, including tracking spend against phasing and ensuring accurate resource allocation. Demonstrated understanding of vendor contracting workflows, including managing MSAs, SOWs, and POs, with the ability to support teams through end-to-end operational processes. Excellent project management skills within medical affairs, with a proven ability to drive complex initiatives and meet deadlines across cross-functional teams. Strong leadership and collaboration skills, with experience working in high-performance environments across pharma, biotech, or life sciences consulting. Effective communicator, able to engage and influence stakeholders at all organizational levels. Strategic thinker who can translate business and medical objectives into clear operational plans and deliverables. Knowledge of pharmaceutical industry regulations, compliance standards, and best practices in medical affairs. Travel is estimated at 10-20% Seniority level

Seniority level Mid-Senior level Employment type

Employment type Full-time Job function

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