Director, North America Medical Affairs

Director, North America Medical Affairs

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S and BAND-AID that you already know and love. Science is our passion; care is our talent.

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage and have brilliant opportunities waiting for you! Join us in shaping our futureand yours.

The Director, North America Medical Affairs has a broad range of responsibilities that include providing strategic leadership and managing and leading in the development of medical affairs strategies and brand development activities for high priority need states. The Director is accountable for both United States and Canada Medical Affairs activities and strategies including country medical affairs plan development. The Director may also have responsibilities for coordination with regional medical affairs in medical affairs development and support of brand development globally.

Key Responsibilities

• Under the guidance of Segment Medical Lead, guide development of Strategic Medical Brand Plan and execute medical strategies to support product innovation, regulatory approvals, and marketing efforts.
• Provide medical affairs strategy in the development of scientific messaging for Kenvue products, ensuring alignment with regulatory, R&D, Safety, and other key stakeholders.
• Recruit, develop and manage high performing Medical Affairs talent for United States and Canada.
• Guide the strategy for country medical affairs plan for United States and Canada and provide impactful medical strategy to commercial, HCP engagement and Regulatory partners.
• Provide impactful medical affairs strategy and therapy area expertise for new claims development, evaluating global innovation and NPD opportunities.
• Oversee preparation and review of scientific documents including but not limited to Aggregate Safety Reports, CCDSs and company publications.
• Develop strategy for and work closely with project teams in designing and executing product approval and lifecycle management activities which may include behavioral use studies supporting new drug applications, risk-benefit evaluations, RWE generation and outcomes studies, consumer science studies.

Cross-functional Collaboration

Scientific Expertise

External Engagement

Compliance and Education

Required and Preferred Qualifications

Skills & Competencies

Annual base salary for new hires in this position ranges : $194,650.00 - $274,800.00. This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors.

Competitive Benefit Package

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.