Senior Manager, Clinical Science – Self Care

Kenvue

. Serve as clinical strategy lead for new product innovations and clinical programs across all phases of product development, including planning, design, execution, and reporting of clinical studies for assigned categories .

Posted 9/23/2026full-timeHelsingborg • SwedenSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical strategy development, including leading clinical programs and regulatory submissions, while effectively communicating scientific evidence to support claims. Proven ability to build relationships with stakeholders and manage multiple projects in a global environment.

Highest-signal resume keywords

Clinical Strategy DevelopmentRegulatory Submission ExperienceClaims Substantiation StrategiesClinical Study DesignTeam Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ExecutionClinical Design DevelopmentInvestigator Brochure PreparationClinical Study Report WritingRegulatory Filing DocumentationClaims Roadmap DevelopmentHuman-Centric InnovationBenefit/Risk AssessmentPeriodic Safety Report ReviewOver-the-Counter Product Development

Soft Skills

Excellent Verbal CommunicationExcellent Written CommunicationRelationship BuildingMentoringProject Management

Certifications & Qualifications

PhDPharmDMD

Industry Keywords

Clinical ProgramsHealth Authority InteractionsScientific StakeholdersMedical DevicesCross-Functional Teams

About the role

Key responsibilities & impact

Serve as clinical strategy lead for new product innovations and clinical programs across all phases of product development, including planning, design, execution, and reporting of clinical studies for assigned categories
Represent clinical strategies during health authority interactions
Shape and deliver claims, claims roadmaps, creative claims substantiation strategies, and communication pipelines targeting consumers and healthcare professionals
Act as a claims subject matter expert and contribute recommendations to strengthen claims and science storytelling for cross-functional project teams
Champion a human-centric innovation mindset
Assure timely and quality completion of investigator brochures, study protocols, clinical study reports, regulatory filing documents, and publications of completed research
Build and maintain relationships with internal and external scientific stakeholders to advance research and development
Own clinical evaluation reports for medical devices in development and post-market clinical follow-up studies for in-market devices
Support activities including Core Data Sheet, periodic safety report review, ingredient/product issue management, and benefit/risk challenges

Requirements

What you’ll need

An advanced degree (e.g., PhD or PharmD or MD) is strongly preferred
Experience in mapping out and leading full clinical development programs for regulatory submission is strongly preferred
Experience in developing clinical designs and methodologies, with execution of clinical studies
Experience in developing compelling claims & communication strategies and translating scientific evidence into robust claims substantiation
Demonstrated ability to understand the business context and work closely with commercial business partners in the development of over-the-counter medicinal products
Experience/leadership in a people/team management capacity is a plus
Must have ability and flexibility to work in a global environment
Ability to manage multiple projects and mentor junior colleagues
Excellent verbal and written communication skills