Sample Management Scientist
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Job Location:
Monthly Salary:
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Laboratory SettingJob Description
This is a fully onsite role based at our customers site in Stevenage UK.
At Thermo Fisher Scientific youll 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.
Thermo Fishers clinical research business is a leading global contract research organization and world leader in serving science. We are passionate deliberate and driven by our mission to enable our customers to make the world healthier safer and cleaner.
Within our Analytical Services team we have a functional service provider solution which is a unique partnership that allows our customers to leverage the experience of our staff while allowing you the employee to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company all while maintaining full-time benefits.
Key responsibilities:
The Sample Management Scientist oversees the lifecycle of clinical samples ensuring their accurate and compliant management to support clinical and bioanalytical activities. This role involves handling sample receipt storage transfer documentation and disposal in alignment with regulatory and ethical standards.
- Sample handling and inventory management: The role includes laboratory tasks such as receiving clinical samples importing manifests into the Laboratory Information Management System (LIMS) and maintaining sample inventory control and reconciliation. Samples are stored in qualified units according to study and SOP requirements.
- Sample tracking and coordination: Accurate tracking of sample locations status and conditions is maintained within the LIMS. The manager coordinates sample transfers to internal analysts ensuring traceability and chain of custody and aligns sample movements with study timelines and analytical needs.
- Compliance documentation and stakeholder communication: All sample management activities are documented timely and accurately to support inspection readiness under Good Clinical Practice (GCP). The manager liaises with clinical teams sites and external organizations ensures compliance with ethical and regulatory requirements supports audits and adheres to health safety and environmental protocols.
Education and Experience:
- Bachelors degree in lab sciences such as Chemistry Biochemistry Material Science Immunology Biology Molecular Biology or similar
- Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 2 years)
In some cases an equivalency consisting of a combination of appropriate education training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
Knowledge Skills and Abilities:
- Experience supporting clinical studies in a regulated (GCP) laboratory biobanking or sample management environment.
- Handson experience with enterprise sample management LIMS platforms (e.g. Watson LIMS or equivalent).
- Familiarity with endtoend clinical sample lifecycle management including longterm storage biobanking and sample disposition.
- Experience working in an inspectionready environment including exposure to audits or inspections (e.g. FDA MHRA internal QA).
- Understanding of data integrity principles (e.g. ALCOA) as applied to clinical sample documentation and electronic systems.
- Demonstrated experience performing clinical sample management activities within a laboratory environment including sample receipt inventory management storage transfer and disposal.
- Proven experience using a sample management Laboratory Information Management System (LIMS) to enter maintain and reconcile sample data including sample manifests and randomization information.
- Working knowledge of Good Clinical Practice (GCP) requirements as they apply to clinical sample handling documentation and traceability.
- Experience performing work in compliance with applicable ethical and regulatory requirements relevant government regulations and controlled Standard Operating Procedures (SOPs).
- Demonstrated ability to maintain accurate documentation sample traceability and chain of custody to support inspection readiness.
- Experience interfacing with laboratory analysts clinical study teams clinical sites and/or contract research organizations in support of clinical studies.
- Demonstrated commitment to safe working practices and adherence to laboratory health and safety requirements.
Benefits
We offer competitive remuneration annual incentive plan bonus healthcare and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation!
Required Experience:
IC
Key Skills
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
