Study Coordinator - Toxicology

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 team in Alconbury, Cambridgeshire.

Work Schedule: Monday – Friday, 8.30am – 5pm (37.5 hours)

Job Responsibilities

• Coordinate activities of routine and non‑routine studies in compliance with company standards, GLP, and regulatory guidelines.

• Provide administrative and scientific support for toxicology studies, including prestudy tasks such as protocol development, costing, and scheduling.

• Monitor the in‑life progress of assigned studies and interact professionally with clients.

• Provide administrative backup support for Study Directors on day‑to‑day study‑specific tasks.

• Support additional non‑study‑specific activities for key clients as required.

• Assist other functions within Safety Assessment as part of daily duties.

• Ensure study compliance with protocols, SOPs, GLPs, and regulatory requirements.

• Coordinate the study award process.

• Coordinate study team efforts and develop project management skills.

• Plan, prioritize, and manage workload and associated responsibilities.

• Draft protocols and amendments for Study Director review and approval.

• Ensure all client comments on protocols and amendments are addressed promptly.

• Initiate and submit costing and scheduling requests.

• Schedule and participate in pre‑initiation and other study‑related meetings; take and distribute meeting minutes.

Minimum Qualifications

• Relevant national level of education in comparison to High School Diploma, GCSE or equivalent.

Additional Job Standards

• Hold basic knowledge of GLPs, regulatory agency guidelines, and Home Office requirements as applicable.

• Demonstrate strong attention to detail and consistent accuracy.

• Show good communication, interaction, and responsiveness skills.

• Possess basic scientific knowledge and understanding of industry 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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