Do you have fantastic organisational skills and want to work in the growing In Vitro Toxicology team?

Are you looking for a role with training and career progression opportunities?

Do you want to be a part of the world's leading life sciences company?

Labcorp is a leading global life sciences company that includes contract research and developmental services to the pharmaceutical, medical technology, crop protection and chemical industries.

We are looking for a Study Coordinator to work in our In Vitro Toxicology team at our site in Harrogate, North Yorkshire.

This is an exciting opportunity to join a knowledgeable and dynamic team where you will play an integral role in supporting the Aerosol Toxicology group.  Providing administrative and scientific support for an increasing range/number of studies including pre-study tasks (i.e., protocol development, scheduling), monitoring the in-life progress of assigned studies, interacting with clients and preparing report components and QC checking of reports.

Please note, this is a fixed term contract for 12 months and an office based role

As a Study Co-ordinator your main responsibilities will be:

Coordinating the activities of key client studies in compliance with regulatory guidelines

Working closely with Study Directors to support all studies

Drafting study documentation & generating study data

Overseeing report production through finalization and archiving of data

Liaising with clients regarding study issues and working as part of a larger team to ensure the study is completed in a timely manner

What Labcorp can offer you:

Competitive salary and a comprehensive benefits package, including health coverage and contributory pension

Ability to work with a variety of different clients on wide ranging projects

Flexible working and career development opportunities

Education:

Degree Level (Scientific or English degree is preferred.)

OR equivalent industry experience

Experience:

Science background or strong interest in this area

Ideally collating data, report  writing and other administrative experience

Some knowledge of GLP, GCP guidelines, ideally having worked in a highly regulated environment

Excellent computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages including Word and Excel)

Ability to multitask and prioritise workload, with excellent attention to detail

Exceptional communication skills

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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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