Description
We are looking for a dynamic and enthusiastic GCLP-Biobank Laboratory Coordinator to support research active clinical teams within the Royal Free London NHS Foundation Trust.
The role holder will join Research and Development Sample Services (RADSS), one of the largest human sample research facilities in the NHS, helping patients donate human biological samples and giving researchers access to consented samples and linked, anonymised clinical data.
The main purpose of this role is to assist with the collection and biological processing of clinical trial samples for clinical research purposes within the RFL R&D. The post holder will provide biological sample processing support to the R&D Clinical and externally contracted GCLP-Biobank studies.
Responsibilities include:
- Collecting and processing clinical trial samples such as blood, biopsy, saliva, and stool
- Booking samples onto LIMS and biologically processing them
- Shipping and storing samples in accordance with GCLP-Biobank and study-specific SOPs
- Complying with HTA, ICH legislation, and governance requirements
- Assisting in data collection and inputting into LIMS
- Providing administrative support to the GCLP-Biobank Team and studies
- Participating in laboratory audits and general laboratory maintenance
The successful applicant will liaise closely with GCLP-RFL Biobank team members, clinical trial delivery staff, Clinical Research Facility personnel, study sponsor representatives, and central analytical laboratories.
Requirements:
- Degree in a scientific/healthcare-related discipline or equivalent experience
- Evidence of Continuing Professional Development (CPD)
- Displays a professional attitude towards colleagues, study PIs, clinical staff, and others
- Flexible attitude to work, including the ability to take up new tasks when required
- Conscientious attitude to the finalisation of any given task
- Ability to problem-solve and work using own initiative
- Recent experience of handling relevant human material in a routine diagnostic clinical or research laboratory
- Experience of working to Human Tissue Act (2004) guidelines
- Experience of general laboratory maintenance, organisation, and stock management
- Scientific knowledge and technical ability
- Technical competence in sample processing
- A good level of expertise in the operation and routine maintenance of laboratory equipment
- Demonstrable knowledge of regulations governing clinical trials, including Human Tissue Act (2004), Data Protection Act (2018), Medicines for Human Use (Clinical Trial) Regulations (2004), Good Clinical Laboratory Practice (GCLP), and Good Clinical Practice (GCP)
- Competence in a Laboratory Information Management System (LIMS)
- Demonstrable knowledge of audit processes
- Knowledge of medical terminology
- Methodical and accurate approach to work showing excellent attention to detail
- Excellent communication skills both orally and in writing