Scientific Director, Medical Affairs

Role Summary

The Scientific Director, US Medical Affairs will provide strategic scientific leadership and expertise to advance the organization’s medical mission and aesthetics portfolio. This role is responsible for shaping and executing medical affairs strategies, ensuring the generation and dissemination of high-quality scientific and clinical data, fostering engagement with key opinion leaders and external stakeholders, and supporting cross-functional collaboration to maximize the impact of medical initiatives. This position plays a pivotal role in overseeing strategic medical projects that support product and indication development and lifecycle management.

Responsibilities

• Provide strategic leadership in the development and execution of medical affairs initiatives aligned with organizational goals.
• Lead the generation, interpretation, and dissemination of scientific and clinical data for internal and external stakeholders.
• Establish and maintain relationships with key opinion leaders, healthcare professionals, and other external stakeholders.
• Oversee the planning and execution of medical education programs and scientific communications.
• Co-lead internal cross-functional meetings across R&D and commercial to support product development and lifecycle management.
• Identify Insight Trends: Address educational scientific gaps identified through the gathering of feedback from multiple field sources, compile and summarize to provide relevant insights. Communicate trends to the broader therapeutic team.
• Manage and drive key strategic medical projects aligned with franchise brand plan. Responsible for designing a strategically aligned tactical plan, as appropriate for pipeline products including new indications/disease states.
• Develop and curate scientific resources and materials to support external scientific communication, including field medical teams and congresses: (i.e. Congress Booth, Ad Boards, Med Ed) with HCP or EE interactions; educational initiatives (medical education, data, guidelines, and value proposition).
• Represent the organization at scientific conferences, advisory boards, and other external meetings.
• Support lifecycle management for pipeline products and participate in evidence generation planning.
• Actively contribute to and drive medical and brand functional planning including: medical education, EE engagements; and provide strategic medical input into core brand/product strategies. Work with TA Lead to ensure external communication strategies and tactics align with both TA and Commercial Strategies.
• Ensure compliance with regulatory and ethical standards in all medical affairs activities.

Qualifications

• Scientific degree; advanced degree (e.g., PhD, MD/DO, PharmD) preferred.
• 10+ years of clinical, scientific/research, or industry related experience or equivalent required demonstrating strong leadership competencies and proven team-building skills with ability to lead in a global matrixed environment. Substantial understanding of relevant therapeutic area required.
• Knowledge of clinical trial design, results and methodology, regulatory and compliance requirements governing development of promotional and non-promotional materials is desirable.
• Ability to interact externally and internally to support global scientific and business strategy.
• Ability to independently evaluate risk and implement strategies that are compliant with applicable regulatory standards pertinent to the promotion of pharmaceutical products
• Demonstrated analytical, conceptual and administrative skills. Excellent communication skills (written and presentation).
• Flexibility and adaptability to organizational change and market demands. Ability to work in a fast-paced corporate environment. High sense of urgency and commitment to excellence in the successful achievement of objectives.
• Excellent planning and organizational skills. Ability to manage multiple priorities and ability to demonstrate good business judgment.
• Strong Project Management and Teamwork skills to address project risks and issues.
• Ability to influence without direct authority to effectively deliver cross-functional projects.