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 tasksCoordinate packages of studiesDraft protocols and amendments for Study Director review and approvalInitiate scheduling requests and request changes to schedulesTake 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 requestsSupport 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 teamCompetitive salaries and a comprehensive benefits package including health cover and contributory pensionOpportunity 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 studiesExcellent attention to detail and consistent accuracy whilst managing multiple changing prioritiesExperience within genetic toxicology and GLP knowledge is desirableAbility to write and prepare routine and complex study procedures, tables and graphs for reportsExperience 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

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