GCMA Senior Associate
We are Reckitt
Research & Development
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
As an R & D Category Senior Associate you’ll lead innovation within Reckitt's diverse portfolio. Apply your expertise to guide critical research and development initiatives, shaping the future of well-known Reckitt products. In this role, you will blend scientific knowledge with strategic insight to uplift product development, propelling them to meet rigorous healthcare standards. With a focus on cross-functional collaboration and team leadership, your work will directly impact the integrity and success of our products on a global scale.
Your responsibilities
- Independently represent the Medical Science team and act as medical expert for area in cross functional project meetings.
- Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth
- Support and educate teams with understanding of the literature, new clinical data and current medical opinion on category topics for Reckitt products and competitors
- Partner with wider Medical Science team to:
- 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
- Provide input and edit/review Regulatory and Clinical Documents required for global RB 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/projects:- 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 in healthcare or the life sciences is required (e.g. basic science, pharmacy, nursing or medical), with relevance to microbiology considered an advantage.
- Experience in preparing medical or scientific documents to a high standard is essential, and experience of working in or for the Consumer Health industry is highly desirable.
- Ability to write, review and interpret medical and scientific information
The skills for success
What we offer
Equality
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