Principal Scientist, Clinical Science

Principal Scientist, Clinical Science

我们做什么

在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。

我们是谁

我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.

Role reports to：

Associate Director Clinical Research

位置：

North America, United States, New Jersey, Summit

工作地点：

混合

你会做什么

The Principal Scientist, Clinical Science plays a key role in shaping and delivering the global clinical strategy for new product innovations and claim upgrades, supporting study design, execution, data interpretation, and scientific storytelling. This role serves as the clinical subject matter expert on cross‑functional and global teams, ensuring clinical evidence is robust, relevant, and supports meaningful consumer and healthcare professional claims. The Principal Scientist partners closely with internal teams and external investigators to ensure studies are conducted with scientific rigor, regulatory compliance, and adherence to Good Clinical Practice. The position also contributes to claims development, publications, and scientific communications, while actively supporting Kenvue’s Human‑Centered Innovation mindset. 

Key Responsibilities

• Serve as a member of Translational Science Clinical Science teams dedicated to the development and/or deployment of the global clinical strategy for new product or claim upgrade innovation projects, including the design, analysis and interpretation of clinical studies to meet desired claims and communication messages for each innovation project.

• Play a clinical subject matter expert role in understanding the relevant science to provide contributions, translations and/or make recommendations to strengthen clinical-based claims and or science storytelling to cross-functional and global project teams within R&D, including novel clinical designs, endpoints and methodologies.

• Serve as Clinical Study Director and fulfill all associated responsibilities for clinical studies partnering with internal clinical operations team and external clinical research service providers and/or HCP KOLs principal investigators, including adherence to internal policies and procedures and external regulatory requirements ensuring good clinical practice conduct.

• Participate on global, cross functional teams for evaluation of new product ideas and project implementation, providing active scientific contributions and ensuring clinical timeline adherence to overall project timeline.

• Contribute to and translate scientific and clinical knowledge and data for consumer-facing and healthcare professional message development, scientific posters and publications. 

• Actively participate in the Kenvue Human Centered Innovation mindset, contributing as the Clinical Subject Matter Expert in the claims process and claims system.

What We Are Looking For

Required Qualifications

• Required Education: Bachelor's degree with at least 5 years or Master’s/PharmD/PhD degree with 3+ years of Consumer/OTC/pharmaceutical (or equivalent) industry and/or relevant clinical work experience.

• Ensure all clinical activities are conducted in accordance with high ethical and quality standards, as well as all applicable policies and procedures.

• Ability to collaborate, influence, manage routine processes, consider measured risks, and make decisions to drive project progress are critical components of the role.

• Must be able to work independently, think analytically, manage multiple complex tasks and projects, while also being highly detail oriented and organized.

• The ability to work in a matrix environment with cross-functional teams and have excellent verbal and written communication skills is essential.

对您有什么好处

$127,075.00 - $179,400.00

这考虑了许多因素，包括工作地点、候选人的技能、经验、教育水平和其他与工作相关的因素

Kenvue 很自豪能成为一个机会均等的雇主。所有合格的申请人都将根据业绩获得就业考虑，不分种族、肤色、宗教、性别、性取向、性别认同、年龄、国籍或受保护的退伍军人身份，并且不会因残疾而受到歧视。