Project Manager – Clinical Supplies

🔥 8 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 Ghost score 15%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Manage the end-to-end supply chain for clinical trials • Ensure timely and efficient distribution of trial materials • Maintain optimal inventory levels • Collaborate with cross-functional teams to support successful clinical studies • Develop study-specific plans for assigned projects • Coordinate internal team efforts, provide recommendations and identify risks • Update project reports and spreadsheets • Integrate clinical supplies activities into the supply chain strategy and ensure GxP compliance • Participate in training on new regulations • Represent the department internally and externally at meetings, strategic projects and initiatives • Mentor and guide junior team members • Participate in process improvement initiatives • Maintain existing tools and identify improvement opportunities • Participate in bidding and bid defense opportunities and address client supply-chain requests, questions and concerns

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 5+ years of comparable experience • Clinical trial/drug development experience • Good understanding of clinical supply operations • Solid client building and 3rd party relationship management • Strong English and communication skills, written and verbal • Strong interpersonal, planning, organizational, problem-solving, sense of urgency and decision-making skills • Effective leadership and team-building skills • Strong working knowledge of Microsoft Office suite • Strong customer focus and attention to detail • Ability to work in a team environment and independently with little guidance • Ability to provide high-quality customer service • Ability to access and use in-house and off-the-shelf computer software • Ability to travel domestically and internationally occasionally

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Ongoing training on new regulations • Opportunity to participate in process improvement initiatives • Mentoring and guidance opportunities • Occasional domestic and international travel

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