Overview
GCMA Manager – Germ Protection (Kingston upon Hull, East Yorkshire, GB, HU1 1AA)
We are Reckitt
​Research & Development​
In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals – all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
This role is integrated within the Global Category Medical Affairs team, responsible for medical science and evidence generation activities during the development and throughout the entire life cycle of Reckitt Germ Protection topical products.
The post-holder is responsible for all relevant medical science team and activities relating to the personal care categories with a focus on topical medicines and medical devices, alongside cosmetics, biocides and general products. The role works with GMS Leads/ Director and brand team to drive commercial success by generating and applying medical insights to deliver high quality evidence that results in safe, efficacious and meaningful innovation to consumers.
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Location: This role can be based at our sites in Hull or Slough, UK
Salary: Competitive Salary plus benefits including Car Allowance, Performance Bonus, Private Medical, 10% Pension Contribution, Annual Salary Review, Sharesave Scheme and more.
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Closing Date: 23rd October 2025
Your responsibilities
The position is accountable to the GMS Lead/Director and finally to the CMO, working closely with others as part of the matrix. The role interacts as appropriate with other internal functions including Clinical, Regional Medical, R&D, Safety, Quality, Regulatory and Compliance (SQRC), Marketing, Medical Channel etc. The role also interacts with external partners including key opinion leaders. Manage the preparation, maintenance and execution of test scripts as required. Work in close collaboration with Information Systems on implementation, change control and testing.
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- Independently represent the Medical Science team and act as medical expert for area in cross-functional project meetings
- Manage the delivery of activities, and contribute to the career progression, of a Medical Science team
- Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growthÂ
- Drive education and understanding of the literature, new clinical data and current medical opinion on category topics for Reckitt products and competitors
- Support development and drive execution of strategic evidence plans to deliver high quality evidence that results in safe and efficacious products. Â Evidence plans may involve clinical testing, field studies or interaction with external experts.
- Provide strategic medical input in category development leading brand science for product innovation and claims
- Proactively partner with the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives
- Provide ideas/concepts for constructing the product pipelines (e.g. new products, new combinations, new technologies, novel evidence generation techniques)
- Provide medical support and oversight for educational and promotional activities
- Manage medical aspects of registration and development of Reckitt products globally
- Manage delivery and edit/review of Regulatory and Clinical Documents required for global Reckitt product development and registration activities.  These include but are not limited to: briefing documents, common technical document (CTD) clinical overviews and summaries, switch applications, integrated summaries of safety and efficacy, investigators’ brochures, clinical documents such as Study Protocols and Informed Consent Forms; clinical evaluation reports (CERs) and other Medical/Regulatory documents including Claim Memos
- Manage internal and external responses, and quality of medical documentation for given area
- Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation
- Conduct systematic literature searches/reviews and prepare responses as necessary
- Edit and proof reading of text written by other team members and providing constructive feedback
- Ensure that working documents and other appropriate documentation are updated and current
The experience we're looking for
- Bachelor’s Degree preferably associated to healthcare or the life sciences (eg basic science, pharmacy, nursing or medical) is required
- Postgraduate qualifications preferred; plus experience in relevant post-graduate experience
- Experience in the medical and pharmaceutical / consumer health industry knowledge is required. Â Medical Affairs experience is preferred.
- Experience in personal care product development including topical medicines, cosmetics, general products and biocides would be an advantage
- Experience in systematic searches, reviewing scientific data, and preparing medical or scientific documents (e.g. post graduate experience in relevant science, publications and experience in medical writing, systematic review and clinical data appraisal) to a high standard is highly desirable.Â
- Knowledge of skin science and how topical personal care formulations interact with the skin; experience compiling evidence strategies including in vitro¸ ex vivo and in vivo methodologies, information management and regulatory requirements and an understanding of healthcare compliance and guidelines is desirable. Proven ability to generate, analyse and interpret scientific and clinical data is required.
- Previous experience of work in New Product Development, or experience of clinical development, with examples of successful product launches
- Experience managing KOLs and running Ad Boards would be an advantage
- Ability to manage multiple projects and products simultaneously to ensure timely, on-target and within budget accomplishment of tasks.
- Demonstrated stakeholder management, and matrix management experience in previous roles
- The Candidate will demonstrate the following capabilities:
- Leadership capability – demonstrated ability to lead and inspire teams and develop and mentor individuals and allocate resource strategically and according to the portfolio priorities.
- Strategic Thinking – maintains competitive advantage by carefully considering the issues and competing priorities within a situation, program or portfolio and then developing a strategy that includes the strategic application of available principles, tools and systems.
- Business Acumen – Understands the implications of decisions related to human, financial, material and information resources, from a business perspective and uses this knowledge to plan, implement and manage clinical research within R&D.
- Project Management – Demonstrates the discipline of risk-based planning, organising and managing resources to bring about the successful completion of specific project goals and objectives in accordance with defined quality and time-based metrics.
- Team or line management experience
- Strong skills in managing multiple projects simultaneously with an ability to prioritise appropriately.
- Track record of building strong internal and external networks.
- Demonstrated ability to manage complexity and cultural diversity.
- Strong interpersonal, verbal and written communication skills.
- Thrives working in fast paced, innovative environment while remaining flexible, resourceful and reliable.
The skills for success
What we offer
Equality
IMPORTANT: Before applying for this role, please make sure you have the right to work in the country where the role is based. Unless it clearly stipulates within in the job advert above that the hiring company is looking to or able to sponsor applicants it is deemed that the hiring employer will only consider applications from those able to comply with and work in the country where the role is based.













