Job Details
Job title: Investigator, Sample Management (Grade 7)
Location: Stevenage
Contract length: 12 months
Role Overview
The role Investigator, Sample Management will be responsible for planning, coordinating, and overseeing all operational activities required to manage the lifecycle of human biological samples. This person will work closely with cross‑functional teams to ensure that all samples are collected, processed, stored, and shipped according to protocol requirements, applicable regulatory standards and in accordance with GSK policies and procedures.
Key Responsibilities
- Develop and maintain detailed sample management plans and protocols for each non‑clinical study.
- Work closely with cross‑functional teams (internally and externally) to ensure that all sample collection, processing, storage, and shipping activities are conducted in accordance with protocol requirements and applicable regulations.
- Manage all aspects of the sample lifecycle, including collection, processing, storage, and shipping.
- Ensure that all samples are tracked and stored correctly, and that all documentation is maintained in accordance with GSK policies and procedures.
- Work closely with laboratory personnel to ensure that all samples are processed and analyzed in a timely and accurate manner.
- Maintain detailed records of sample collection and management, including chain of custody documentation and sample inventory logs.
- Ensure that all sample‑related activities are conducted in accordance with GSK policies and procedures, as well as applicable regulations.
- Work with external vendors to coordinate sample shipping and storage activities.
- Participate in the development and implementation of new sample management technologies and systems.
- Ensure that all sample‑related activities are conducted in a safe and compliant manner.
Requirements
- Bachelor's degree in a related field (e.g., biology, chemistry, or a related life science field).
- At least 3 years of experience in sample management or a related field.
- Strong understanding of sample management protocols and regulations.
- Experience working with cross‑functional teams in a clinical research environment.
- Excellent organizational skills and attention to detail.
- Strong communication and interpersonal skills.
- Ability to work independently and manage multiple projects simultaneously.
- Experience working with laboratory information management systems (LIMS) is a plus.
- Willingness to work flexible hours as needed to support study activities.
Inclusion at GSK
GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
