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Senior Scientist

Job in Reading, Berkshire, RG1, England, UK
Listing for: Kenvue
Full Time, Part Time position
Listed on 2026-09-01
Job specializations:
  • Healthcare
    Clinical Research, Medical Science Liaison
Salary/Wage Range or Industry Benchmark: 55000 - 110000 GBP Yearly GBP 55000.00 110000.00 YEAR
Job Description & How to Apply Below

Working mode:
Hybrid, 1-2 days per week on-site

Duration: 12 months

Hours:
Full-time, 37 hours per week

Pay rate range:
Competitive hourly rate

The Senior Scientist is responsible for managing medical affairs programs, coordinating data analyses and reporting and communicating scientific results. You will support medical operations, develop educational materials, and ensure compliance with regulatory requirements:

roles and responsibilities
  • Translate scientific data into actionable insights
    , analysing need-state science, brand and competitor evidence and emerging trends to inform cross-functional partners and Teams.
  • Analyse emerging medical trends with real-world evidence and clinical trial data to influence product lifecycle management, medical strategy, and training programs
  • Support innovation and product development
    , contributing scientific analysis, literature reviews, claims input, and technical assessments to global pipeline and lifecycle projects.
  • Enable global evidence generation and medical programs
    , including expert mapping, insight gathering, data-generation proposals, and dissemination of results via publications and presentations.
  • Develop high

    - quality scientific and educational materials
    , including training content, clinical summaries, and HCP-focused programs that support global medical communication.
  • Prepare technical content for regulatory documentation
    , contributing to submissions, RFIs, aggregate safety reports, and updates to product information (eg SmPCs).
  • Execute medical communication plans
    , ensuring accurate, evidence-based messaging across internal, HCP, and consumer-facing channels.
  • Ensure compliance with scientific and regulatory standards
    , implementing processes that uphold medical governance, ethical requirements, and safety-reporting obligations.
  • Participate in product safety, periodic reporting and labelling programs, including updates to Company Product Information
  • Collaborate and share expertise across the organisation
    , maintaining strong stakeholder connections and contributing to product safety programs, labelling updates, and a culture of scientific excellence.
how to succeed
  • Bachelor’s degree or equivalent in Life Sciences or a related scientific or healthcare field.
  • 6 or more years of progressive experience in medical affairs or related healthcare roles.
  • Demonstrated expertise in managing medical affairs programs, including safety reporting and data management.
  • Excellent understanding of clinical data, data analysis, and regulatory compliance.
  • Excellent communication skills for effective interaction with healthcare professionals and internal teams.
  • Experience in planning and executing clinical educational activities and medical communications.
  • Strong organizational skills with the ability to manage multiple projects and deadlines.
  • Capability to maintain collaborative relationships with cross-functional teams and stakeholders.
Desired Qualifications
  • Demonstrated ability to synthesize complex clinical data into clear, compelling narratives that influence medical and commercial stakeholders.
  • Proven expertise in designing and executing innovative medical education programs and scientific communication strategies.
  • Strong analytical mindset, proficient use of digital tools, AI and data analytics to enhance medical insights, program design and decision-making
  • With experience leveraging real-world evidence and health economics to inform medical decision-making.
  • Exceptional interpersonal and leadership skills, with a track record of successfully managing cross-disciplinary teams and fostering collaborative partnerships.
  • Proven ability to develop and implement policies and procedures within a medical or pharmaceutical environment.

This role offers a very competitive hourly rate. This contract will run initially for 12 months.

you are welcome here

Kenvue is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

About Kenvue

At Kenvue, we realise the extraordinary power of everyday care. Built on over a century of heritage and…

Position Requirements
10+ Years work experience
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