Project Manager – Clinical Supplies

🕒 October 15

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 Ghost score 20%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 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 clinical studies • Develop study-specific plans for assigned projects • Coordinate internal team efforts, provide recommendations and risk updates, and maintain project reports and spreadsheets • Integrate clinical supplies activities into the supply chain to support logistics strategy and 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/or 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, or equivalent combination of education, training, and directly related experience • Clinical trial/drug development experience • Good understanding of clinical supply operations • Solid client building and 3rd party relationship management • Strong English and written and verbal communication skills • 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-standard customer service • Ability to access and use in-house and off-the-shelf computer software • Ability to travel domestically and internationally occasionally • Ability to meet physical requirements including frequent stationary work, repetitive hand movements, mobility, occasional bending/twisting, and light to moderate lifting of 15–20 lbs • Regular and consistent attendance

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Ongoing training on new regulations • Opportunities to participate in process improvement initiatives • Opportunities to participate in strategic projects and initiatives • Mentoring and guidance opportunities • Fully remote, hybrid, or office-based work options in listed country locations