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Associate director clinical research

Northampton
Jr United Kingdom
Associate director
Posted: 24 August
Offer description

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Associate Director Clinical Research, Northampton

Client: SRG

Location: Northampton, United Kingdom

Job Category: Other

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EU work permit required: Yes


Job Views:

1


Posted:

22.08.2025


Expiry Date:

06.10.2025


Job Description:

* Job Title – Associate Director, Clinical Research
* Contract Length – ASAP until end of May 2026

Key Responsibilities

* Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned.
* 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 (with support from Clinical Research Director).
* Support peer review publications/input to clinical section of regulatory dossiers to ensure scientific robustness from a medical and scientific standpoint.
* Responsible for the design, implementation, reporting, interpretation, disclosure, and publication of company-sponsored clinical studies following external (e.g., GCP) and internal policies.
* Contribute clinical content to regulatory submissions and other engagements for clinical research activities.
* Support clinical/medical due diligence for external opportunities from a clinical research perspective.

Related Experience

* Minimum 8 years’ experience in clinical research/drug development in the Pharmaceutical/CRO or Healthcare industry, preferably in Consumer Healthcare / FMCH / Pharmaceutical sectors. Consumer Health care experience is highly preferred.
* Experience within Oral Health, Wellness, Pain relief, or Respiratory is an advantage.
* Proven ability to liaise and influence both internally and externally.
* Ability to work effectively in a multi-functional team.
* Excellent verbal and written communication skills.
* Strong scientific writing skills.
* Track record of delivering clinical development programs/studies/clinical evidence activities.
* Experience representing an organization with external stakeholders.
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