Clinical Trial Job at Syneos Health, UK | Life Sciences | Apply Now
If you are an early-career life sciences graduate or an analytical logistics professional looking to step into clinical operations, this full-time role at Syneos Health is an exceptional career move. Located at our advanced regional office in Farnborough, England, this position places you at the critical intersection of clinical supply chain logistics, current Good Manufacturing Practice (cGMP), and international trial compliance. For organized professionals searching for a high-impact Clinical Trial Job, this position offers hands-on exposure to batch manufacturing records, customs clearance coordination, and global supply forecasting. It serves as an elite launchpad to kickstart a long-term Syneos Health career and stands out as a premier selection for anyone tracking a competitive Life Sciences Job within a leading global Contract Research Organization (CRO).
- Job Position: Clinical Trial Supplies Associate
- Location: Farnborough, England, United Kingdom
About The Company
Syneos Health® is a premier, world-leading fully integrated life sciences services organization built to accelerate customer success. Operating across a massive international footprint of 25,000 colleagues, the company blends a clinical development powerhouse with a commercialization engine. Over the past five years alone, Syneos Health has worked on 94% of all Novel FDA-Approved Drugs and 95% of EMA-Authorized Products across more than 200 studies. This specific role sits within the Clinical Solutions division in Farnborough, UK. Whether deployed in a full-service environment or an integrated Functional Service Provider (FSP) partnership, team members apply a drug development mindset to navigate global supply complexities. Joining this supplies unit embeds you into an inclusive, highly collaborative culture where your daily oversight of investigational medicinal products (IMPs) directly impacts trial milestone velocities and patient progress worldwide.
Clinical Trial Job – Key Responsibilities
The Clinical Trial Supplies Associate executes essential administrative, auditing, and tracking activities under the guidance of the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL).
Your core distribution planning, inventory auditing, and compliance duties include:
- Distribution & Return Coordination: Assisting in the functional design and execution of logistics plans for the initial distribution, localized re-supply, and final return or destruction of clinical trial supplies.
- Batch Disposition Support: Reviewing batch manufacturing, packaging, and labeling records to support the technical assessment and formal release of clinical trial materials.
- Inventory Forecasting Assistance: Supporting the continuous review and forecasting of clinical inventory levels across global depots in tight cooperation with project teams and external vendors to advance this Clinical Trial Job.
- Customs Clearance Triage: Facilitating international customs documentation and shipping verifications to ensure investigational drugs pass safely across borders without study delays.
- Trial Master File Curation: Maintaining accurate tracking tools, updating inventory logs, and preserving complete regulatory documentation in line with internal standard operating procedures (SOPs).
- Cross-Functional Communication: Maintaining proactive, professional interactions with internal project coordinators and external third-party suppliers to support your Syneos Health career.
Qualifications & Profile Requirements For Clinical Trial Job
Syneos Health seeks a structured, detail-oriented coordinator who demonstrates excellent organizational habits and can manage multiple logistical priorities in a fast-paced environment.
- Required Academic & Legal Criteria:
- Educational Foundation: A completed Associate’s Degree (or equivalent institutional level of education), preferably focused on the Life Sciences or a related natural science field.
- Linguistic Mastery: A high level of competence and professional fluency in written and verbal English is mandatory for this UK-based Life Sciences Job.
- Software Competency: Strong proficiency navigating standard Microsoft Office applications (specifically Word, Excel, and Outlook).
- Desired Experience & Technical Assets:
- Prior professional work experience or internship exposure within a Contract Research Organization (CRO), pharmaceutical company, or biotechnology business unit is preferred.
- A foundational, theoretical understanding of Good Clinical Practice (GCP), ICH guidelines, Good Manufacturing Practice (GMP), and other regional clinical trial supply regulatory frameworks.
- Excellent interpersonal skills and a proactive, collaborative approach to problem-solving within matrixed teams.
- Travel Flexibility: Willingness and physical capability to accommodate occasional domestic or international travel as required by project needs (up to 5%).
In short, the Clinical Trial Supplies Associate position at Syneos Health is a definitive route to translating your life sciences background or logistics skillset into a premium global clinical operations asset. Securing an appointment here allows you to step past general administrative tasks and take direct, frontline charge of the batch record reviews, inventory forecasts, and distribution paths that keep international clinical pipelines running safely. If you reside in or can commute to Farnborough, meet the academic parameters, and possess an uncompromising eye for detail, apply today to secure this premier Clinical Trial Job, launch an exceptional Syneos Health career, and lock in this outstanding Life Sciences Job.
