Study Coordinator

3 weeks ago

Harrogate, United Kingdom Labcorp Full time

**Job Overview**:
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?

Do you want the opportunity to make a difference and work on a variety of studies within a global organization?

Labcorp Drug Development is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical, crop protection and chemical industries. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market.

At our site in Harrogate, we are looking to recruit a Study Coordinator to join our Aerosol Research and Development section within Genetic and Molecular Toxicology.

The Study Coordinator is responsible for coordinating the activities of Aerosol R&D studies and you will work alongside the Study Directors, providing scientific and administrative support in the conduct, writing and organization of multiple studies.

As Study Coordinator you will:

- Draft and compile reports to include preparing the draft study report and data tables that include basic statistical analysis using data/table generation programs/spreadsheets
- Learn to coordinate report production by ensuring that all client comments are addressed and documented in a timely manner, preparing final reports and amended finals ready for dispatch to client including archiving procedures of study raw data and final report, through to the final mailing out of the report
- Verify that the study schedule accurately reflect the requirements of the protocol along with learning to draft protocols and amendments for Study Director review and approval
- Assist Study Directors in monitoring critical phases of routine studies, reviews data, identifies problems, and ensures the study is conducted according to protocol specifications, SOPs and other procedures/regulations
- Assist in hosting client visits and liaise with the client
- Perform QC check of reports to assure completeness and accuracy prior to formal peer reviews, where appropriate
- Take responsibility for general study coordination tasks to include scheduling shipping of samples, invoicing, sorting orders for studies, provide administrative backup support for the Study Directors as appropriate

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 remote working after training
**Education/Qualifications**:

- Bachelor’s degree or equivalent experience. Degree and/or experience in technical writing, document production/publishing, and/or science preferred
**Experience**:

- Experience in either Aerosol R&D or genetic toxicology or a client facing role with project management skills
- Skilled in concise/technical writing, requiring little third-party review or editing
- Demonstrates excellent communication, time management and organisational skills with the ability to manage multiple studies
- Good I.T / software skills to include Microsoft Office
- Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
- GLP knowledge and/or experience desirable

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