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 Senior 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 In Vitro Inhalation 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 permanent full time office based role.

As a Senior Study Coordinator your main responsibilities will be:

Providing backup support for Study Director on day to day study specific activities or tasks.

Coordinating packages of work as appropriate, taking responsibility for one or two major clients.

Reviewing data output from the lab areas for data acceptability and compliance with protocol. Identifying and managing the resolution of any deficiencies in conjunction with the Study Director.

Drafting summary results documents, as required

Writing and preparing routine and complex study procedures, tables and graphs for the report.

Acting as alternative contact for the Sponsor in the absence of the Study Director.

Additional Client Management responsibilities as appropriate for at least one key client. These may include but are not limited to: status updates, invoicing queries, scheduling, specific client requirements.

Maintaining awareness of specific software used in study conduct and training/instructing less experienced Study Coordinators in the use of this software, as required.

Maintaining familiarity with routine and specialised study procedures.

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:

Scientific background, ideally within a similar role

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:

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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