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Principal Scientist - Clinical Research
View: 144
Update day: 14-04-2024
Category: R & D IT - Software
Industry: Consumer Services
Position: Mid-Senior level
Job type: Full-time
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Job content
Site Name: Switzerland - Nyon, UK - Surrey - Weybridge, USA - New Jersey - Warren, Weybridge – HeadquartersPosted Date: Sep 27 2023Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, NeoCitran, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question.Your RoleAs an Associate Director Clinical Research, you will support the delivery of clinical development excellence of clinical studies and other clinical evidence gathering activities sponsored by Haleon in line with specific category/ sub-category project strategies.This role will provide support to cross-functional category/ sub-category / Business Unit teams on clinical research, new opportunities/business development and R&D strategies. The role will require significant interaction with several internal teams including but not limited to Category and Business Unit Medical Affairs, Clinical Operations, Biostatistics & Data Management as well as external groups/ individuals such as investigators/ academic researchers, Clinical Research Organizations and Health Care Practitioners to help achieve company objectives and to build Haleon reputation.Your Tasks- Provide scientific/technical input to category/ sub-category/Business Unit clinical development plans
- Design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including Rx-to-OTC switch programs and medical devices.
- Implement novel research methodologies in line with ICH GCP to generate clinical evidence for impactful claims in support of successful product launches, brand positioning and messaging.
- Be responsible for the design, implementation, reporting, interpretation, disclosure and publication of clinical studies detailed in research programs supporting consumer healthcare/category products and to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements.
- Be responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
- Be responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.
- Minimum 5 years’ experience in clinical research/drug development in the Pharmaceutical or Healthcare industry, preferably in a Consumer Healthcare / FMCH / Pharmaceutical business Consumer Health care experience is greatly preferred.
- Previous experience in innovative product/therapy area including Rx-to-OTC switch programs and medical devices is an advantage.
- Demonstrated experience and proven track record of delivering clinical development programs/clinical studies/clinical evidence gathering activities
- Demonstrated experience representing an organization with external stakeholders
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Deadline: 29-05-2024
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