Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Study Coordinator to join our Toxicology team in Harrogate, North Yorkshire.

Work Schedule: Monday – Friday, 8.45am – 5pm (37 hours)

Job Responsibilities

• Providing administrative and scientific support for toxicology studies, including pre-study tasks (e.g., protocol development, costing, scheduling), monitoring the in-life progress of assigned studies, and interacting with clients
• Providing administrative backup support for Study Directors on day to day study-specific activities or tasks
• Learning to ensure study compliance with the protocol, standard operating procedures, Good Laboratory Practices, and other regulatory guidelines
• Learning to plan, prioritize, and manage a workload and the associated responsibilities
• Serving as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable
• Learning to draft protocols and amendments for Study Director Review and approval
• Scheduling and participating in pre-initiation and other study-related meetings, as required, and taking and distributing preinitiation meeting minutes
• Learning to draft and submit appropriate documents to the IACUC/AWERB for approval
• Learning to address and review quality assurance audits relating to protocols and amendments and reports (as applicable), with oversight. Following up with appropriate personnel to ensure all necessary document/data clarifications are completed in the specified timelines
• Assisting with hosting client visits
• Assisting Study Director by ensuring that study documentation such as Literature Reviews and Animal Order Forms are in place

Minimum Qualifications

• BSc, preferably Life Science degree

Additional Job Standards

• Some experience or knowledge in Toxicology/Study Coordination or a client facing position
• Ability to demonstrate excellent communication and time management skills
• Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
• Knowledge of GLPs, regulatory agency guidelines and Home Office requirements

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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