Clinical Supply Chain Manager - Logistic

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