Associate Medical Director

Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981 we have dedicated our focus and passion to the human bodys largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives we are advancing dermatology for every skin story.

We look for people who focus on getting results embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all they must be passionate about doing something meaningful for consumers patients and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company we embrace diversity and respect the dignity privacy and personal rights of every employee.

At Galderma we actively give our teams reasons to believe in our bold 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 professionalsultimately 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 plancovering abstracts posters and manuscriptsaligned 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 engagements.

• Support medical review of US promotional and non-promotional materials by ensuring scientific accuracy and compliance as part of Medical Legal and Regulatory (MLR) or Promotional Review Committee (PRC) processes.

• Participate in the planning and execution of advisory boards symposia and scientific events including content development logistical support and engagement with key opinion leaders (KOLs).

• Manage relationships with external medical communications vendors and medical writers to ensure high-quality timely and aligned deliverables across all projects.

Qualifications and Competencies:

• Advanced degree (PharmD PhD or MD) required with strong preference for candidates with expertise in dermatology immunology or allergic diseases; experience with biologics and/or rare diseases is highly desirable.

• Minimum of 3 years experience in medical affairs or medical communications within the pharmaceutical or biotech industry; experience in field medical roles strategy development or relevant consulting is a plus.

• Demonstrated ability to develop and execute medical strategies and clearly communicate complex scientific concepts to diverse audiences.

• Experience driving medical initiatives from concept through execution is an asset.

• Proven ability to manage multiple projects prioritize effectively and deliver high-quality results within tight timelines.

• Strategic mindset with the ability to align medical communications with broader business objectives.

• Strong attention to detail and a commitment to scientific and regulatory accuracy.

• Collaborative team player with the ability to work cross-functionally and engage stakeholders at all levels.

• Proactive adaptable and comfortable working in a fast-paced evolving environment.

• Excellent interpersonal communication and collaboration skills with a proven ability to engage both internal and external stakeholders.

• Solid understanding of the US regulatory landscape and adherence to ethical standards and compliance guidelines.

• Willingness to travel as needed to support business and medical affairs responsibilities.

Location and Travel:

This is a Boston based position with occasional travel required for conferences and meetings as needed.