Senior Scientist, Medical and Scientific Affairs-OTC

Location: Warren Township

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.

Our trusted portfolio of brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

About the Role As a Senior Scientist, Medical & Scientific Affairs - OTC, you will support Haleon's portfolio of over-the-counter medicines by advancing the science behind trusted brands through evidence generation, scientific communications, claims development, and regulatory support. Working across multiple therapeutic areas, you will collaborate with cross-functional teams to translate complex scientific data into meaningful insights that support brand strategy, product registration, and lifecycle management activities.

This role is ideal for a scientist or healthcare professional who enjoys applying scientific expertise across a broad range of consumer health categories. This role includes support for regulatory submissions and evidence packages that help bring innovative consumer health products to market.

Key Responsibilities Support the development and execution of medical strategies, including evidence generation, claims substantiation, scientific communications, medical education, and benefit-risk assessments.

Conduct critical evaluation, interpretation, and synthesis of clinical and scientific data to support medical and business objectives.

Support the preparation of scientific and medical content for regulatory submissions, product registrations, evidence dossiers, and lifecycle management activities.

Contribute to the development of study plans, protocols, literature reviews, and evidence summaries.

Develop evidence-based responses to scientific and medical inquiries from internal and external stakeholders.

Partner with regulatory, marketing, legal, and cross-functional teams to ensure scientific accuracy and compliance across product communications.

Support the development and review of promotional and non-promotional materials using an evidence-based approach.

Monitor emerging scientific research, healthcare trends, and competitive activity across multiple therapeutic areas.

Coordinate scientific advisory boards, consultant engagements, and external expert interactions.

Build relationships with internal stakeholders and external experts to support scientific strategy and evidence generation.

Basic Qualifications Bachelor's degree in Life Sciences, Pharmacy, Healthcare, or a related scientific discipline.
1-3 years of experience in Medical Affairs, Scientific Affairs, Clinical Research, Regulatory Affairs, or a related field.

Preferred Qualifications Advanced degree such as PharmD, PhD, MD, or other healthcare-related doctorate.
4+ years of experience in Medical Affairs, Scientific Affairs, or related functions within consumer healthcare, pharmaceutical, or biotechnology industries.

Experience supporting FDA or other regulatory submissions.

Experience evaluating clinical data and developing scientific evidence packages.

Ability to interpret and communicate complex scientific information across multiple therapeutic areas.

Stro…