Clinical Trial Supplies Associate – Farnborough, UK
Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return).
Job Responsibilities
- Assists in the development of systems and plans for distribution, re‑supply, and return of clinical trial supplies.
- Supports the review of batch manufacturing and packaging records to enable batch disposition.
- Supports review and forecasting of inventory levels for all clinical trial supplies, in cooperation with project teams and project vendors.
Qualification Requirements
- Associate’s Degree (or equivalent) level of education, preferably focused on life sciences.
- Experience in a contract research organization (CRO), pharmaceutical or biotechnology company is preferred.
- Knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practice, and other applicable regulatory requirements.
- High level of competence in English language.
- Proficiency with MS Office applications.
- Ability to travel as necessary (up to 5%).
EEO and Disability Accommodation Statement
Further, nothing contained herein should be construed to create an employment contract. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.
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