Associate Medical Director, Medical Affairs, Skin Health & Beauty

Associate Medical Director, Medical Affairs, Skin Health & Beauty

私たちがしていること

Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.

Who We Are

私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.

Role reports to:

Director, Medical Affairs MD

Location:

North America, United States, New Jersey, Summit

勤務地:

ハイブリッド

あなたがすること

The Associate Director, Medical Affairs, Skin Health & Beauty is responsible for medical affairs responsibility for the Kenvue’s Skin Health & Beauty portfolio. This individual will bring diligent experience, medical/clinical thought leadership, medical/health expertise, health insights, digital/data science competencies, creative strategic foresight and strong influencing skills to lead without authority. This individual will apply their medical & scientific expertise to guide and inform R&D leaders as well as other medical, scientific, claims, scientific engagement, pre-clinical, and business leaders.

Key Responsibilities:

• Help develop and implement strategic medical plans to advance the medical affairs division, ensuring alignment with company goals and brand objectives

• Collaborate with cross-functional teams including Commercial, Regulatory, Safety, Translational/Clinical Science, Public Affairs & Clinical Operations to help shape product and claims development and launch initiatives, leveraging expertise in skin health and beauty

• Participate in strategic organization of Skin Health Publication, Scientific Communication, and Claims Development strategies

• Collaborate with cross-functional teams to help execute strategic medical brand planning

• Work closely with managers to organize and execute cross-functional medical affairs deliverables which includes but is not limited to: strategy sessions, scientific output, advisory boards, R&D input, safety input, and/or marketing input

• Contribute to scientific publications and presentations to showcase expertise in the field

• Maintain accurate records of project information and ensure proper retention of records and raw data

• Provide medical review for promotional review content as required, and be involved in medical writing support for company core data sheets, drug safety analyses, and publications

• Additional responsibilities for products may include aiding with a wide range of Regulatory classifications (New Drug Applications (NDAs), Monograph Drugs, Medical Devices and combination products).

• This individual may serve as a medical monitor and or study director to clinical studies/consumer research studies

• Stay updated on the latest industry trends and advancements in medical affairs related to skin health and beauty, incorporating new insights into research and development projects  Provide guidance and mentorship to junior team members, fostering a culture of continuous learning and growth

What we are looking for

Required Qualifications

• US-based medical leader (MD/DO or equivalent) or FMCG (Foreign Medical College Graduates; MD/DO or equivalent)

• Dermatology experience is highly preferred

• Minimum 5-7 years of proven experience in medical affairs (Rx, OTC or Cosmetics), and/or clinical research and clinical development

• Strong communication skills and interpersonal skills

• Ability to collaborate with cross-functional teams and present scientific findings

• Proven ability to think strategically and drive results

• Experience in mentoring and developing team members is a plus

Desired Qualifications

• Strong understanding of medical affairs program management and strategic initiatives

• Experience in leading cross-functional teams and collaboration

• Highly organized and efficient

• Proven track record of contributing to R&D projects, advisory boards, scientific engagement and presentations

#LI-GC1

それは何ですか

$197,200.00 - $278,400.00

これは、勤務地、候補者のスキル、経験、教育レベルなど、多くの要素を考慮に入れています。その他の仕事関連の要因.

Kenvueは機会均等雇用者であることを誇りに思っています。人種、肌の色、宗教、性別、性的指向、性同一性、年齢、出身国、または保護された退役軍人の地位に関係なく、すべての資格のある応募者は、能力に基づいて雇用の検討を受け、障害に基づいて差別されることはありません。