Location: Moreton, Wirral (Hybrid – 50/50)
Rate: £34 per hour
Contract: 12 months
PAYE
Atrium (EMEA) are supporting a global biopharma company looking for a highly experienced Clinical Supply Chain Manager to join a fast-paced, global clinical operations environment. This is a critical “hypercare” role where you will play a key part in ensuring life-changing clinical trials stay on track through seamless, end-to-end supply chain execution.
If you thrive under pressure, are hands-on with logistics operations, and can “hit the ground running,” this is an exciting opportunity to make a real impact from day one.
Key Responsibilities
* Oversee end-to-end clinical supply logistics, ensuring timely delivery of investigational medicinal products (IMP)
* Act as the single point of contact for all logistics activities across study teams and stakeholders
* Drive execution of stock transfer orders (STOs) and manage shipment flows across global networks
* Monitor critical shipments, proactively resolving delays and mitigating risks
* Coordinate with external partners (e.g. depots, CMOs, logistics providers) to maintain seamless supply
* Align closely with study timelines, enronllment needs, and key clinical milestones
* Deliver weekly reporting on logistics performance, risks, and mitigation plans
* Escalate issues effectively to ensure continuous supply during high-risk or urgent phases
Technical Skills Required
* Bachelor’s degree in Supply Chain, Life Sciences, Engineering, or related field
* 10+ years’ experience in clinical supply chain logistics (global trial exposure preferred)
* Strong hands-on experience with STOs, shipment execution, and issue resolution
* Proven ability to work in high-pressure, time-critical environments (“hypercare”)
* Excellent problem-solving and strategic thinking capabilities
* Strong communication skills – able to collaborate across global teams and external partners
* SAP knowledge and familiarity with supply chain systems
* High level of independence – able to contribute effectively after a short induction
Why Join?
* Work on critical clinical trial programs with global impact
* Collaborate with cross-functional international teams
* Take ownership in a high-visibility, high-impact role