Study Manager

Our client is one of Europe’s leading providers of research services for molecular pathology; spatial transcriptomics and proteomics; histopathology and quantitative image analysis. Serving a global client base, the company provides GLP and GCP compliant services for preclinical and clinical studies. Our client has built a leading reputation in the growing field of spatial biology, having validated a range of best-in-class technology platforms from our strategic partners, Nano String, Lunaphore, Akoya Visiopharm and Pathcore.

Based in Herefordshire, the team is friendly and passionate about working with exciting new technology and developing innovative methods and techniques.

• Substantial knowledge and practical experience of IHC techniques, including manual and automated methods, ideally a minimum of four years
• Able to communicate (in written and verbal form) clearly, confidently and expertly
• Highly motivated, confident, pro-active and able to work independently
• Science graduate with a relevant PhD

• Experience working in industry either at a biopharma company or within a CRO
• Experience of multiplex immunofluorescence platforms (Akoya and/or Lunaphore), Visiopharm and bioinformatics for multi-omic data
• Substantive experience of GCP and/or GLP quality management systems
• Strong drive to get head and to take greater responsibility in the future

This is an exciting role within our Molecular Pathology team, leading and supporting experimental and regulatory studies. The role will include developing and validating methods for multiplex immunofluorescence methods, IHC and RNAScope. Responsibilities will evolve over time and include elements of the following:

• Liaison with clients/Sponsors on technical requirements
• Development of study plans and reports
• Development and validation of IHC methods, including multiplexed methods
• Supporting technicians within the team
• Participation in regulatory and Sponsor QA audits
• Evaluation of new technologies and process improvements
• Contributing to scientific marketing materials
• Presenting at industry conferences
• Ensuring compliance with GLP and GCP requirements

The role presents several opportunities to develop professional skills in leading commercial studies within a regulatory framework; and in working directly with cutting-edge, novel technology.