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.
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.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months with a start date in September 2024.
A unique opportunity has arisen for a Laboratory Scientist to make a move into a more data focused role with a leading bioanalytical CRO in Macclesfield!
Joining a dynamic team, you'll will be utilising your analytical and problem-solving skills to check scientific data and calculations.
You'll be supporting study directors and projects leaders in data analysis ensuring all data is in compliance with regulatory standards, aiding with the timely delivery of projects to clients.