Experienced Study Coordinator - Genetic Toxicology

Do you have scientific knowledge in Genetic Toxicology paired with project management skills?

Are you looking to work in an exciting new role where you can develop and grow to your full potential?

At our site in Harrogate, North Yorkshire, we are looking to recruit an experienced Study Coordinator to join our Genetic Toxicology department within the Reporting and Study Coordination team.

The Study Coordinator is responsible for coordinating the activities of Genetic Toxicology studies and you will work alongside the Study Directors, providing scientific and administrative support in the conduct and organisation of multiple studies and study types. Please note, this is an office based role.

As a Study Coordinator you will work as part of the coordinator team to:

• Provide support for Study Directors on day-to-day study specific tasks
• Coordinate packages of studies
• Draft protocols and amendments for Study Director review and approval
• Initiate scheduling requests and request changes to schedules
• Take responsibility for general study coordination tasks including scheduling shipping of samples, acquisition of test article and relevant documentation, and preparing documents for review e.g. solubility assessments and dose requests
• Support with the preparation of study reports summarising study data as required

What we can offer you:

• Exposure to new and novel procedures with excellent career development opportunities in a supportive, growing team
• Competitive salaries and a comprehensive benefits package including health cover and contributory pension
• Opportunity for flexible and/or some remote working after training

Education:

• Bachelor's degree or equivalent experience

Skills / Experience:

• Demonstrates excellent written and verbal communication, time management and organisational skills with the ability to manage multiple studies
• Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
• Experience within genetic toxicology and GLP knowledge is desirable
• Ability to write and prepare routine and complex study procedures, tables and graphs for reports
• Experience in technical writing, document production/publishing, and/or science preferred

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

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Client-provided location(s): Ripon, United Kingdom

Job ID: labcorp-2526476_1316070705

Employment Type: OTHER

Posted: 2025-08-09T04:14:03