Galderma
Overview
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 body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. 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. Position
Associate Medical Director, Nemolizumab Location: Hybrid Greater Boston Area Responsibilities
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 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 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. 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.
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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 body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. 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. Position
Associate Medical Director, Nemolizumab Location: Hybrid Greater Boston Area Responsibilities
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 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 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. 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.
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