Syneos Health
Clinical Trial Supplies Associate ** Farnborough, UK **

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Clinical Trial Supplies Associate ** Farnborough, UK **
Clinical Trial Supplies Associate – Farnborough, UK
Syneos Health® is a leading fully-integrated life sciences services organisation built to accelerate customer success. We partner with innovators across the drug development and commercialisation continuum, helping them navigate complexity, anticipate change, and accelerate progress.
Our Clinical Solutions team members prioritise a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and shape tailored solutions. Whether as a Functional Service Provider or in a Full-Service environment, you’ll collaborate with passionate, driveing teams to help customers achieve their goals.
With 25,000 current employees across a global workforce, we are:
- Focused on developing our people through career progression, line management support, training, peer recognition, and rewards.
- Committed to an inclusive culture, underpinned by our purpose “Driven to Deliver” – ensuring everyone feels authentic and engaged.
- Continuously improving to ensure we deliver value to both our customers and patients, shaping the future of healthcare collaboratively.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
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About the Role
The Clinical Trial Supplies Associate supports the logistics, distribution, and management of clinical trial supplies, reporting to the Clinical Trial Supplies Manager or Project Lead.
Responsibilities
- Assisting with logistics plans: Support the development of systems and plans for distribution, re-supply, and return of clinical trial supplies.
- Batch review and compliance: Support the review of batch manufacturing and packaging records to facilitate batch disposition.
- Inventory management: Collaborate with project teams and vendors to review forecasts and maintain optimal inventory levels for all clinical trial supplies.
Requirements
Educational Background
- Associate’s degree (or equivalent) preferred in life sciences.


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Experience
- Experience in a Contract Research Organisation (CRO), pharmaceutical, or biotech company is beneficial.
- Familiarity with clinical trial logistics, supply chain processes, and Good Clinical Practice (GCP) preferred.
Technical Knowledge
- Strong understanding of ICH guidelines, Good Manufacturing Practice (GMP), and regulatory requirements applicable to pharmaceutical trial supplies.
- Data accuracy and roi management (WEST BUSINESS AWARENESS).
Language Skills
- High level of competence in English.
Technical Skills
- Proficient with MS Office applications (Excel, Word, etc.).
Administrative & Flexibility
- Ability to travel as required (up to 5% of the time).
Note: Responsibilities may change as determined by Syneos Health. Applicants with equivalent qualifications may be considered.
For additional details about Syneos Health and other opportunities, visit Syneos Health.
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