Exciting opportunity for an experienced Study Director to uphold a pivotal role within a successful and expanding team!
Your main responsibility will be to oversee a range of GLP/GCP regulated studies as well as develop, validate and apply LC-MS/MS methods. You will work as Study Director on allocated sponsor studies and will be responsible from initial protocol through to final report. Using your exemplary communication and interpersonal skills, you will also train and supervise junior staff as well as liaise directly with external customers.
Applications are invited from experienced Study Directors with a strong background within a bioanalytical laboratory. You will be competent developing novel methods from scratch, be able to supervise and train junior staff and have an excellent understanding of laboratory regulations.
The lab is exceptionally well-equipped, working with cutting edge LC-MS/MS technology on bespoke bioanalytical projects.
Apply to VRS now to be considered for this exciting new opportunity!
Bioanalysis, bioanalytical analysis, drug development, Liquid Chromatography, Mass Spectrometry, LC, MS, LCMS, LC-MS, sample preparation, extraction, SPE, solid phase extraction, method development, method validation, Study Director, GLP, GCP, North East, Yorkshire, York, Leeds, VRS5786AW