The split role involves working flexibly across all pathology areas.
Clinical Trials Function:
1. Communicate and collaborate with the research team to facilitate effective study delivery.
2. Maintain positive relationships and integrated research delivery with clinical teams.
3. Maintain and organize essential trial documentation.
4. Comply with Good Clinical Practice at all times.
5. Assist with data entry and respond to data queries.
6. Work with other team members to cover workload for annual leave and ensure continuity of study delivery.
7. Keep mandatory training up to date.
8. Engage with the challenge of learning and change.
9. Work closely alongside Biomedical Scientists, the Pathology Reception Team Leader, and the Research and Innovation department.
Laboratory Function:
1. Use various IT systems and software, including Laboratory computer system (LIMS), Trust EPR, Analyser interfaces, QC software, and QPulse Quality Management system (write SOPs, perform audits, distribute documents).
2. Monitor analysers in the department, dealing with errors on samples, maintenance on the analysers, replenishing reagents and consumables, and basic troubleshooting/fault finding.
3. Complete all required documentation for maintenance and error logging.
4. Manage stock with BMS staff, perform stock takes, order reagents and consumables via the Cardea ordering system, sign for deliveries, receipt goods delivered, unpack, verify if appropriate, and ensure paperwork is complete before placing in the appropriate storage area in an orderly manner.
5. Communicate effectively with staff from various wards, departments, and other laboratories, as well as Trust IT, Trust transport drivers, porters, Blood Bikers, and the Blood Sciences Team.
6. Pay attention to detail to pick up and appropriately record errors, ensuring patient samples are accurately identified, tested, and results recorded or transcribed.
7. Focus for long periods and organize tasks in priority order.
8. Demonstrate computer literacy and be expected to write SOPs and perform audits as needed.
9. Multi-task, keep calm and focused in high-pressure situations, and be flexible and organized during business continuity.
Requirements:
Recent NHS experience in Clinical Trials and up-to-date qualifications such as Good Clinical Practice and Transport of Dangerous Goods are expected.
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