FSP IRT Project Manager - Global Clinical Supplies
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (33.0%).
Occupation Type
Business and financial project management professionals
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£56,500
(£28.97 per hour)
Occupation rate applies
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Description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
ocation/Division Specific Information
This position will be embedded within a client-dedicated FSP team supporting Global Clinical Supplies. The role supports a growing portfolio of clinical studies, including onboarding of a new sponsor to the 4G Clinical IRT platform. The successful candidate will operate in a highly collaborative, cross-functional environment, partnering with sponsors, IRT vendors, and internal teams across regions to ensure effective IRT and investigational product management execution.
Role Summary
Standard (Mon-Fri)
Environmental Conditions
Office
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
ocation/Division Specific Information
This position will be embedded within a client-dedicated FSP team supporting Global Clinical Supplies. The role supports a growing portfolio of clinical studies, including onboarding of a new sponsor to the 4G Clinical IRT platform. The successful candidate will operate in a highly collaborative, cross-functional environment, partnering with sponsors, IRT vendors, and internal teams across regions to ensure effective IRT and investigational product management execution.
Role Summary
The IRT Project Manager will provide portfolio-level IRT project management oversight across multiple clinical studies and IRT platforms within an FSP delivery model. The role supports both standard IRT Managed Services and studies requiring enhanced or supplemental IRT oversight. The IRTPM will partner closely with Global Clinical Supplies, Clinical Operations, sponsors, and IRT vendors to ensure effective IRT execution, supply continuity, and alignment with study needs. Hands-on experience with the 4G Clinical IRT platform is required to support studies utilizing 4G and to address scenarios where additional operational involvement is needed beyond standard managed services.
Key Responsibilities
IRT Project Management and Portfolio Oversight
Key Responsibilities
IRT Project Management and Portfolio Oversight
- Provide project management oversight for IRT activities across a portfolio of clinical trials and IRT platforms.
- Serve as the primary IRT point of contact for assigned studies, ensuring alignment between sponsor expectations, managed services scope, and FSP responsibilities.
- Support governance, documentation, and adherence to defined RACI models across IRT engagements.
IRT Managed Services Interface
- Act as the liaison between study teams and IRT Managed Services to ensure services are delivered in line with contractual scope.
- Monitor IRT Managed Services performance, risks, and deliverables across assigned studies.
- Identify gaps between managed services scope and study needs and escalate or mitigate appropriately.
- Collaborate with Global Clinical Supplies PMs on threshold strategies, resupply planning, and enrollment-driven forecasting as needed.
- Support inventory, expiry, and shipment oversight in coordination with GCS PMs, particularly when IRT activities directly impact supply continuity.
- Assist with exception management, including manual shipments and depot-to-depot transfers, when required.
- Coordinate across sponsors, IRT vendors, depots, packaging partners, and internal teams to ensure seamless execution.
- Support studies with complex communication matrices or limited sponsor-side IRT resources.
- Proactively identify IRT and supply-related risks across the portfolio and support mitigation planning.
- Contribute to process improvements, lessons learned, and best practices related to IRT and supply integration.
- Support internal planning related to workload, resourcing, and financial considerations for IRT activities.
- Apply hands-on knowledge of the 4G Clinical IRT platform to support studies requiring deeper operational involvement.
- Support or perform ongoing 4G configuration oversight, system monitoring, and operational adjustments when required by study complexity or sponsor needs.
- Provide subject matter expertise for 4G-related troubleshooting, issue resolution, and vendor interactions.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.