Project Manager – Clinical Supplies

Thermo Fisher Scientific

. Manage the end-to-end supply chain for clinical trials .

Posted 10/15/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing the end-to-end supply chain for clinical trials, ensuring compliance with GxP regulations while maintaining optimal inventory levels and effective client relationship management. Proven ability to lead cross-functional teams, mentor junior members, and implement process improvements.

Highest-signal resume keywords

Clinical Trial ManagementSupply Chain OperationsClient Relationship ManagementLeadership and Team BuildingMicrosoft Office Suite

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ManagementSupply Chain OperationsInventory ManagementProject CoordinationProcess ImprovementRegulatory ComplianceData AnalysisBidding and Bid DefenseLogistics StrategyProblem Solving

Soft Skills

Communication SkillsInterpersonal SkillsOrganizational SkillsDecision-Making SkillsSense of Urgency

Certifications & Qualifications

Bachelor's Degree or Equivalent

Industry Keywords

Clinical TrialsGxP ComplianceDrug DevelopmentCross-Functional CollaborationCustomer Service

About the role

Key responsibilities & impact

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 and provide recommendations, risks, and project report/spreadsheet updates
Integrate clinical supplies activities into the supply chain to support logistics strategy and GxP compliance
Participate in ongoing 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
Work in production, office, or home-based environments
Perform physical and computer-based tasks, communicate with diverse groups, plan work schedules, and manage variable workloads

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
5+ years of previous 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 both 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 focus on customers and attention to detail
Ability to work in team environment and independently with little guidance
Ability to provide customer service with the highest standards of quality and excellence
Occasional domestic and international travel
Ability to access and use various computer software
Ability to perform under stress and multi-task
Regular and consistent attendance

Benefits

Comp & perks

Global team environment
Collaboration and development opportunities
Ongoing training on new regulations
Opportunity to participate in process improvement initiatives
Opportunity to participate in strategic projects and initiatives
Mentoring and guidance opportunities