Director, North America Medical Affairs

Join to apply for the Director, North America Medical Affairs role at Kenvue

Overview

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®. Science is our passion; care is our talent.

Role

Location : North America, United States, New Jersey, Summit. Work Location : Hybrid. Reports To : Head of Global Safety Risk Assessment.

What You Will Do

The Director, North America Medical Affairs has a broad range of responsibilities that include providing strategic leadership and managing the development of medical affairs strategies and brand development activities for high-priority needs 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 coordinate with regional medical affairs in medical affairs development and support of brand development globally.

Key Responsibilities

• Strategic Leadership : 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

What’s In It For You

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.

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.

Seniority level

Employment type

Job function

Industries

Referrals increase your chances of interviewing at Kenvue by 2x

Get notified about new Director Medical Affairs jobs in Summit, NJ.

#J-18808-Ljbffr