Do you have fantastic organisational skills and want to work in the pharmaceutical industry supporting a growing Metabolism team?

Are you looking to take the next step in your scientific career?

Do you want to be a part of the world's leading drug development company?

If so, read on!

Labcorp is a world-leading, life science contract research organization with a mission to improve health and lives.

Recognized as one of Forbes’ World’s Best Employers 2024 and named one of The World’s Most Admired Companies 2025 by Fortune, Labcorp is seeking to hire a Senior Associate Study Coordinator to join our Metabolism department at our site in Harrogate, North Yorkshire.

As a Senior Associate Study Coordinator, you will be responsible for coordinating the activities of routine and non-routine studies in compliance with appropriate company standards and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved in a timely, efficient and quality manner. 

This is an exciting, new opportunity for someone with industry experience looking for a non-lab based role where you can remain close to the science!

Duties Include:

Drafting protocols, amendments and study schedules as appropriate using study outline or client supplied information 

Reviewing study compliance against protocol, SOP and regulatory agency guidelines 

Preparing study schedules based on input from Study Director (SD)/Principal Investigator (PI), places information into databases and communicates work plan to laboratory personnel and support groups, as applicable

Participating in and assisting SD/PI with pre-initiation and other study related meetings as required 

Reviewing progress and study status against initial work plan – maintains CMS with accurate schedules

Proactively communicates and interacts with study team (SD’s and operational staff) to ensure key milestones are achieved 

Serving as the primary contact in communication and interaction with other departments and clients as applicable 

Maintaining well documented, organised and up-to-date study files including study schedule, protocol and correspondence

Taking responsibility for and driving report production through finalization, including archiving of data as appropriate

Preparing for and participating in routine client visits under direction of the SD/PI. Hosting routine client visits and interacting/communicating with client as necessary

We Offer:

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

The opportunity to work in a global team with a variety of different clients on wide ranging projects

Exposure working with multiple different areas of the business

Flexible working with possibility of hybrid working after completion of training

Unrivalled opportunities to develop a successful career in the scientific industry in a supportive team with full training provided where required

A culture of CARE with access to wellbeing programs and various employee resource groups

Education:

BSc however experience may be substituted for education

Skills / Experience:

Demonstrable experience working in the scientific industry, preferably in pre-clinical/non-clinical setting

Organised with the ability to work accurately and to deadlines

Team orientated with strong communication skills

Data collection/analyzing, writing reports, archiving or other administrative experience is advantageous

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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