Associate Medical Director

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing 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.

Associate Medical Director, Nemolizumab

Location: Hybrid Greater Boston Area

Position Overview:

We are seeking a driven Associate Medical Director to join our dynamic US Medical Affairs team. This pivotal role will support the strategic execution of the comprehensive medical plan for nemolizumab in atopic dermatitis and prurigo nodularis. The ideal candidate will support, shape, and implement US-specific medical strategies; develop and execute the US scientific communications plan and content; lead the execution of the US publication plan; and create content addressing the evolving competitive landscape. Additional responsibilities include contributing to medical review processes and developing deep expertise in nemolizumab. You will collaborate closely with cross-functional partners, including internal and field medical teams, to ensure impactful engagement with healthcare professionals—ultimately helping to advance patient care in medical dermatology.

Key Responsibilities:

Reporting to the Head of US Medical Affairs for nemolizumab and working in close collaboration with the US Medical Director and Senior Manager of Medical Affairs, the US Associate Medical Director will be responsible for the following:

• Support the US Medical Affairs (USMA) strategic plan for nemolizumab by leading the development and execution of the US medical communication and education strategy. Ensure alignment with the overall Medical Affairs objectives, brand narrative, and applicable regulatory and compliance guidelines.

• Implement comprehensive, multi-channel medical communication and education plans that deliver accurate, timely, and impactful scientific messaging tailored to key healthcare professional (HCP) audiences.

• Lead the creation, production, and periodic updates of scientific and educational resources, including publications, slide decks, standard response documents (e.g., FAQs), internal training materials, and other medical content. Ensure scientific accuracy, consistency, and alignment across all medical affairs deliverables.

• Develop and manage detailed content and project plans to coordinate activities across matrixed teams including Medical Affairs, Commercial, Compliance, Legal, and external partners. Collaborate with Clinical Development, Regulatory Affairs, and other stakeholders to translate complex clinical data into clear, effective communications.

• Develop and implement a US-focused publications plan—covering abstracts, posters, and manuscripts—aligned with the global publications strategy. Work closely with Global Medical Affairs to ensure integration and consistency across regional and global plans.

• Develop and execute a US-focused publications plan, including abstracts and posters at prioritized congresses, aligned with the global publications plan. Collaborate with global medical affairs to ensure consistency and integration into local plans and support development of forward-looking US medical communications and related training

• Conduct in-depth scientific and competitive landscape analyses to generate internal training content and strategic insights for US Medical Affairs and cross-functional teams.

• Ensure all medical communication and education initiatives adhere to applicable regulatory requirements, industry guidelines (e.g., Good Publication Practice), and internal SOPs, maintaining the highest standards of scientific integrity and ethical conduct.

• Regularly evaluate KPIs and gather insights from advisory boards, structured insight-generation activities, congresses, CME data, and medical information channels to continuously refine the US medical communications and education strategy.

• Attain deep scientific and clinical knowledge of nemolizumab through critical review of clinical study reports and integrated summaries of safety and efficacy. Serve as a key internal resource for scientific and product expertise.

• Contribute to the planning and execution of medical education activities at key national and regional congresses, including symposia, booth content, and peer-to-peer engage