Life Science Jobs at Labcorp
Labcorp Drug Development is seeking a Study Coordinator to join its Toxicology team at the Harrogate site in North Yorkshire. This is a full-time, on-site role. The Life Science Jobs at Labcorp are ideal for proactive individuals with a strong interest in toxicology who enjoy working with people and are ready to take the next step in their scientific career. The position offers hands-on exposure to preclinical toxicology studies at a leading global Contract Research Organization.
Job Details:
- Job Title: Study Coordinator
- Job ID: 263849
- Category: Research and Development
- Employment Type: Full-Time
- Location: Harrogate, North Yorkshire, United Kingdom
- Work Mode: On-site (with potential flexible working after training)
About the Company:
Labcorp Drug Development is a world-leading Life Sciences Contract Research Organization (CRO) providing comprehensive laboratory testing and drug development services to the pharmaceutical, crop protection, and chemical industries. With a mission to improve everyday lives, Labcorp supports the development of essential medicines while maintaining the highest scientific and regulatory standards across global operations.
Educational Requirements for the Study Coordinator Role:
- Bachelor’s degree (BSc), preferably in a Life Science discipline. Relevant experience may be considered in place of formal education.
Key Responsibilities:
- Coordinate routine and non-routine toxicology studies in compliance with company standards, regulatory guidelines, and Home Office requirements in the Life Science Jobs at Labcorp
- Provide administrative and scientific support for studies, including protocol development, costing, scheduling, and in-life monitoring
- Support Study Directors with day-to-day study-specific tasks and documentation
- Ensure study compliance with protocols, SOPs, GLP, and regulatory requirements
- Act as a point of contact for internal departments and clients alongside the Study Director
- Draft study protocols and amendments for review and approval
- Address and manage client comments on protocols and amendments in a timely manner
- Schedule, attend, and document pre-initiation and study-related meetings
- Prepare and submit documents to IACUC/AWERB for approval
- Support quality assurance audits and ensure timely follow-up on findings
- Assist with hosting client visits and coordinating study-related logistics
- Ensure key study documentation (literature reviews, animal order forms) is in place
- Prepare shipping documentation, including CITES applications, as required
Skills Required:
- Basic knowledge or experience in toxicology, study coordination, or client-facing roles
- Understanding of Good Laboratory Practices (GLP) and regulatory agency guidelines
- Familiarity with Home Office requirements related to toxicology studies
- Strong written and verbal communication skills
- Excellent time management and organizational abilities
- Close attention to detail with consistent accuracy
- Ability to manage multiple changing priorities effectively
- Strong interpersonal skills and ability to work collaboratively across teams
Benefits of the Life Science Jobs:
- Exposure to a wide range of pre-clinical toxicology studies
- Opportunity to collaborate with multiple departments, from client management to reporting teams
- Clear career progression pathways within toxicology and Safety Assessment
- Competitive salary with a comprehensive benefits package, including health cover and a contributory pension
- Strong focus on learning, development, and long-term career growth
- Supportive team environment with mentoring opportunities
- Access to wellbeing programs and employee resource groups
- Inclusive, equal-opportunity workplace culture
