R&D Biomedical Scientist.

Job overview

This role is only open to applicants that currently work within an NHS Trust within the Hampshire and Isle of Wight Integrated Care System (HIOW ICS)

The post holder will be a HCPC-registered Biomedical Scientist responsible for supporting pathology R&D services related to clinical trials and research activities across the Trust. They will perform scientific investigations and ensure pathology-related tasks within clinical trials are conducted according to protocols. The post holder will assist Associate practitioner in maintaining the quality, compliance, and operational efficiency of the research and development service.

The post holder will work collaboratively with staff across all Trust sites and departments, ensuring delivery of high-quality service in compliance with regulatory standards such as MHRA and UKAS. You will work closely with senior staff within the department and organisation to ensure that R&D related governance issues are effectively managed within the department.

Main duties of the job

• To ensure all pathology aspects of studies are conducted according to study protocol and laboratory manual.
• Assist in the preparation, handling, labelling, storage and dispatch of trial samples such as blood, urine, and other biological materials in line with study protocols.
• Perform pre-analytical and analytical procedures, ensuring compliance with trial-specific requirements and laboratory standards.
• Participate in the processing, dispatch, and storage of samples for clinical trials or research studies.

Quality and Compliance

• Ensure laboratory processes related to research and clinical trials comply with MHRA and UKAS standards.
• Support the development and maintenance of Standard Operating Procedures (SOPs) for clinical trials and research activities.
• Participate in internal and external quality assurance schemes to maintain compliance with Trust and

national standards.

Governance and Documentation

• Maintain accurate and up-to-date records for all research activities, including a register of active studies, sample logs, and dispatch details.
• Ensure data confidentiality, compliance with the Data Protection Act, and adherence to Good Clinical Practice (GCP) guidelines.
• Assist in the preparation of reports on research pathology activities and Key Performance Indicators (KPIs).

Detailed job description and main responsibilities

Further information about the Trust and this role can be found on the Job Description and Person Specification document attached.