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⚡ Source: ReedRef: 56904629

Supply Chain Logistics Manager

Hays Specialist Recruitment Limited·Wirral·Posted 1 week ago
💰 £34/hour
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Job description

Original text imported from Reed

Position Summary
The Clinical Supply Chain Logistics Manager is responsible forproviding end-to-end hyper-carelogistics oversight for assigned clinical supplyprograms. This role ensures uninterrupted, compliant, and timely delivery ofInvestigational Medicinal Products (IMP) to support critical clinical trialmilestones.
The role serves as the single point of contact (SPOC) for logisticsacross designated studies and works closely with Study Teams, Regional DeliveryLeads (RDLs), Trial Supply Managers (TSMs), and external partners. A strongfocus is placed on execution, proactive risk management, escalation, andtransparency, particularly during high-risk or time-critical phases such asstudy start-up, database lock, and major supply transfers.

Pay Rate £34ph PAYE basic.
Type:Max of 50% at home &50% in the office 50/50 Hybrid WorkPolicy
Terms: 1 month notice period
Interview:1-2 rounds ofinterviews
Location:Moreton, GB
Duration:12 Months
Hrs/Wk:35.00

Key Responsibilities

  • Provide day-to-day operational oversight of logistics activities across assigned clinical supply programs.
  • Monitor and manage Stock Transfer Orders (STOs) across internal and external networks.
  • Drive shipment execution by expediting releases and shipments to meet study timelines.
  • Prioritize urgent, high-risk, and patient-critical deliveries.
  • Act as the primary logistics contact for Study Teams, RDLs, and TSMs.
  • Ensure clear, proactive, and two-way communication with all stakeholders.
  • Resolve logistics issues and provide timely updates on shipment and supply status.
  • Align logistics execution with study priorities, enrolment forecasts, and milestone timelines.
  • Continuously track STOs across internal systems and external depots.
  • Identify risks related to supply availability, release timelines, transport, and handovers.
  • Monitor shipment lifecycle and intervene proactively in the event of delays or deviations.
  • Collaborate closely with external partners including CMOs, packaging vendors, depots (e.g., Catalent), and logistics providers.
  • Partner with Trial Supply Managers (TSMs) to align on release schedules.
  • Anticipate downstream logistics impacts of delays and proactively implement mitigation strategies.
  • Enable timely shipment execution through proactive planning and coordination.
  • Prepare and deliver weekly hyper-care status reports (STO health, shipments, risks, and mitigations).
  • Maintain visibility of critical paths, open issues, and priority shipments.
  • Escalate supply risks, delays, and systemic issues to leadership and governance forums.
  • Drive transparency and data accuracy across logistics operations.


Qualifications & Experience

  • Bachelor's degree in Supply Chain, Life Sciences, Engineering, or a related discipline.
  • Proven experience in clinical supply chain logistics, preferably within a global clinical trial environment.
  • Strong hands-on experience managing:
  • Stock Transfer Orders (STOs)
  • Shipment execution and tracking
  • Issue resolution in complex supply chains
  • Demonstrated ability to operate effectively in high-pressure, time-sensitive environments.
  • Strong stakeholder management and cross-functional collaboration skills.
  • Excellent communication and problem-solving abilities.
  • High attention to detail with strong organizational and prioritization skills.
  • Experience working with external partners (CMOs, depots, logistics providers) is highly preferred.


How to Apply: If you're interested in thisrole, click 'apply now' to forward an up-to-date copy of your CV, or call usnow. If this job isn't quite right for you, but you are looking for a newposition, please contact us for a confidential discussion about your career.

Hays Talent Solutions is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

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Key skills

AI-extracted from the job advert

Must-have skills
Clinical Supply Chain ManagementStock Transfer Orders (STO)Investigational Medicinal Products (IMP)Clinical Trial LogisticsBachelor's degree in Supply Chain or Life SciencesPharmaceutical Supply Chain Experience
Nice-to-have
CMO ManagementCatalent Depot ExperienceGlobal Clinical Trial EnvironmentLife Sciences Engineering Background
Soft skills
Proactive CommunicationRisk ManagementProblem SolvingStakeholder ManagementAttention to DetailTime ManagementEscalation Management
SpeedCV AI

Application advice

5 AI-generated recommendations to maximise your chances.

1

⭐ Highlight your clinical supply chain experience prominently as this role specifically requires oversight of Investigational Medicinal Products (IMP) logistics

2

📊 Quantify your STO management experience: 'Managed 150+ Stock Transfer Orders monthly, achieving 98% on-time delivery'

3

🌐 Emphasise your pharmaceutical industry experience, particularly with CMOs, packaging vendors, and depots like Catalent

4

🎯 Showcase your proactive risk management skills with specific examples of preventing supply chain disruptions during critical trial phases

5

🤝 Demonstrate your stakeholder management abilities across Study Teams, TSMs, and RDLs in previous clinical trial environments

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Suggested CV bullets

3 bullets our AI drafted for this specific advert, mirroring its ATS keywords.

How to tailor your CV

Add these 3 bullets under your most recent experience:

  • Managed 200+ Stock Transfer Orders monthly across 15 global clinical trial sites, achieving 97% on-time delivery of Investigational Medicinal Products
  • Led logistics coordination with 8 CMO partners and external depots including Catalent, reducing supply chain delays by 35% during critical study phases
  • Implemented proactive risk management protocols for IMP shipments, preventing 12 potential trial delays and saving £2.3M in study costs

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Dear Hiring Manager,

Hays' Clinical Supply Chain Logistics Manager position perfectly aligns with my expertise in Investigational Medicinal Products logistics and Stock Transfer Order management across global clinical trial environments. My proven track record in pharmaceutical supply chain operations and experience with CMO partnerships makes me an ideal candidate for this critical role.

My background in clinical supply chain management has equipped me with the skills to provide end-to-end hyper-care logistics oversight whilst maintaining compliance and managing complex stakeholder relationships across Study Teams and external partners.

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Interview questions

10 questions generated from this advert.

Technical

  • How would you manage Stock Transfer Orders across multiple clinical trial sites?
  • Describe your experience with Investigational Medicinal Products logistics
  • How do you track shipment lifecycle across internal and external depot networks?
  • What systems have you used for clinical supply chain management?
  • How would you handle a critical IMP shortage during database lock phase?

Behavioural

  • Tell me about a time you had to escalate a supply chain risk to senior leadership
  • Describe a situation where you prevented a clinical trial delay through proactive logistics management
  • How do you prioritise competing demands from multiple Study Teams?
  • Give an example of how you've managed relationships with external CMO partners
  • Tell me about a time you had to resolve a complex logistics issue under tight deadlines
SpeedCV AINEW

STAR answer examples

Model answers using the Situation-Task-Action-Result framework. Adapt to your own experience.

1Question

Tell me about a time you had to escalate a supply chain risk to senior leadership

During a Phase III oncology trial, I identified a potential 3-week delay in IMP supply due to manufacturing issues at our CMO partner. The situation threatened database lock for 450 patients across 12 sites. I immediately escalated to the Clinical Operations Director with a detailed risk assessment and proposed mitigation plan. I coordinated emergency stock transfers from our European depot, negotiated expedited shipping with our logistics provider, and established daily monitoring calls with the CMO. Through proactive escalation and swift action, we maintained study timelines and avoided a £1.8M delay cost whilst ensuring patient safety remained the priority.
2Question

Describe a situation where you prevented a clinical trial delay through proactive logistics management

While monitoring STO tracking systems, I noticed unusual customs clearance patterns for IMP shipments to our Latin American sites. Rather than waiting for delays to materialise, I proactively contacted our logistics provider and discovered new regulatory requirements that would impact 85% of our shipments. I immediately coordinated with our regulatory team to update documentation, arranged alternative shipping routes through our Miami hub, and communicated revised timelines to 6 Study Teams. This proactive approach prevented a 4-week delay across 3 studies and maintained enrollment targets for 200 patients.

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