In this diverse, multifaceted position, you will call upon your expertise in regulated studies to undertake a broad range of challenging bioanalytical projects for several world-leading organisations. Acting as a scientific point of contact for both internal teams and external clients, your work will focus on the oversight, management, and strategic direction of studies supporting PK, ADA and biomarker analysis, ensuring delivery to the highest scientific and regulatory standards.
The ideal candidate will have:
* A relevant degree (BSc/MSc in Biology or related field)
* Specialist knowledge & experience in bioanalytical techniques, particularly within PK, Anti-drug Antibody (ADA) & Biomarker studies
* Proven experience working to GCP and GLP regulations, including managing and directing regulated studies
* Excellent written and verbal communication skills, with the ability to act as a scientific point of contact
* Strong work ethic and drive to learn
* Candidates with strong experience in either regulated work or biological work are encouraged to apply, as training can be provided for the complementary skill set
This is an excellent opportunity to join a respected organisation, where scientific quality, collaboration, and professional development are genuinely valued.
Please apply now to VRS recruitment to find out more!
Keywords: Project Manager, Study Director, Regulated studies, biology, Biopharmaceuticals, biotherapeutics, immunoassay, ELISA, bioanalysis, analysis, analytical, anti-drug, immunoaffinity, protein, peptide, antibodies, enzyme immunoassay, Gyrolab, MSD, Mesoscale Discovery, Singulex Erenna, radioimmunoassay, AlphaLISA, DELFIA, pharmacokinetic analysis, flow cytometry, mass spectrometry, immunogenicity testing, cytokines, biomarker quantification, GLP, Good Laboratory Practice, GCP, Good Clinical Practice, LIMS, industrial lab, graduate, clinical studies, therapeutics, biomarkers, Suffolk, East Anglia, Cambridge, Cambridgeshire, VRS9441PC
Salary description
£35000.00 - £45000.00 per year