Social network you want to login/join with:
Associate Director Clinical Research, High Wycombe
Client: SRG
Location: High Wycombe, United Kingdom
Job Category: Other
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 (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.
* Contribute clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
* Support clinical/medical due diligence for external opportunities from a clinical research point of view.
Related Experience
* 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.
#J-18808-Ljbffr