About this job

A leading provider of laboratory services to global clinical trials, our client delivers bioanalytical and toxicology programmes from their state-of-the art facility in York.

Partnering with customers across the bioanalytical sector working to optimise programs during the crucial stage of the drug discovery and development process, they give technical insight, expertise and flexibility to provide assay method development and validation for the quantification of drugs, metabolites and biomarkers.

Joining the business as an integral member of the team, you will act as Study Manager for a range of regulated and non-regulated small molecule bioanalytical projects, ensuring these are conducted in compliance with regulatory standards, and are on time and within budget. Utilising previous experience you will lead a small team, ensuring effective performance management and defining responsibilities and objectives as required, as well as overseeing LC-MS/MS method development and troubleshooting.

Applications are invited from accomplished Bioanalytical Study Managers or Study Directors with experience mentoring or supervising a small team. You will also have a strong background undertaking LC-MS/MS small molecule quantitative analyses in support of GLP or non-regulated bioanalytical studies.

In return your will receive a highly competitive salary and comprehensive benefits package, with career advancement opportunities available. In addition, financial assistance with relocation can be offered for the successful candidate.

Please note this is a 100% site-based role in York.

Apply to VRS to be considered today!

Key words: bioanalysis, bioanalytical, Study Manager, Study Director, Team Leader, Leadership, Management, laboratory, LC-MS, LC-MS/MS, GLP, GCP, GxP, analytical chemistry, pharmaceutical, drug development, metabolites, York, Yorkshire, VRS8816AW

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