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Associate Director Clinical Research, weybridge
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Client:
SRG
Location:
weybridge, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Views:
3
Posted:
22.08.2025
Expiry Date:
06.10.2025
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Job Description:
* Title: Associate Director, Clinical Research
* Contract: ASAP until 29-May-2026
* Location: Weybridge Hybrid – approx. 2 days on site
SRG are working with a world-leading consumer company who are seeking an Associate Director, Clinical Research to join the team.
Job Overview
Responsible for leading clinical research activities with a focus on clinical efficacy, effectiveness (through prospective Real World Evidence studies) and other clinical evidence generation activities by ensuring that high quality clinical research expertise is provided to meet state-of-the-art scientific, industry and regulatory standards (as needed).
Lead clinical development evidence generation activities in line with specific category/ sub-category project strategies.
Responsible for the development, 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 company reputation.
Key Responsibilities
* Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned.
* With support from the Clinical Research Director, design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including medical devices, in line with ICH GCP and other regulatory requirements (as needed).
* Support peer review publications/input to clinical section of regulatory dossiers to ensure that they are scientifically robust from a medical and scientific standpoint.
* Responsible for the design, implementation, reporting, interpretation, disclosure and publication of company sponsored clinical studies to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements.
* Responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
* Responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.
Knowledge/ Education / Previous Experience Required
* Advanced Scientific degree e.g. M.S. or MSc in Clinical Science or Medical/Dental or related discipline
* Minimum 8 years’ experience in clinical research/drug development in the Pharmaceutical/CRO or Healthcare industry, preferably in a Consumer Healthcare / FMCH / Pharmaceutical business Consumer Health care experience is greatly preferred.
* Previous experience within Oral Health, Wellness, Pain relief or Respiratory is an advantage.
* Proven ability to effectively liaise and influence internally and externally
* Ability to work in a multi-functional team
* Excellent verbal and written communication skills
* Excellent scientific writing skills
* 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
* Demonstrated competent business acumen
* Excellent verbal and written communication skills in English
* Strong computer literacy including competency in Microsoft Office software
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