Senior Pharmacy Technician - Clinical Trials (Band 5) | Moorfields Eye Hospital NHS Foundation Trust
| Dyddiad hysbysebu: | 12 Ionawr 2026 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | £37,259 - £45,356 per annum pro rata |
| Oriau: | Rhan Amser |
| Dyddiad cau: | 11 Chwefror 2026 |
| Lleoliad: | London, EC1V 2PD |
| Cwmni: | Moorfields Eye Hospital NHS Foundation Trust |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | 7712238/DC-273-7712238 |
Crynodeb
The post holder will carry out the role of Senior Pharmacy Technician for Clinical Trials and will be responsible for the following:
· Assist in the provision, maintenance and development of Clinical Trials Pharmacy Services provided to the Trust.
· Support the Lead Pharmacy Technician for Clinical trials with the day-to-day management and supervision of the pharmacy Clinical Trials services and dispensing activities.
· Assist in the management of the security, recording & maintenance of all Clinical Trial drugs from receipt, storage & return or destruction.
· Ensure that all clinical trials within the Trust are pharmaceutically managed, maintained, and that all current legislation is followed so that research is carried out to the highest standard.
· Train pharmacy, medical and nursing staff on relevant aspects of clinical trials, services and medication.
• Support Lead Pharmacy Technician for Clinical trials with the day-to-day management of the pharmacy clinical trials services.
• Assist with the efficient operation of dispensing services within the Clinical Trials. Ensure clinical trial protocols and SOPs are followed at all times and that the Clinical Trials activity trackers are maintained.
• Ensure the security, recording & maintenance of all Clinical Trial drugs from ordering. receipt, storage, return and destruction.
• Responsible for ensuring that patient returns are appropriately handled, stored and destroyed, and adequate drug accountability is maintained.
• Ensure prompt registration to the IWRS for each new trial, and that the IWRS tracker is updated
• Ensure prompt receipt of shipments and management of temperature excursions according to the trial's specific procedures.
• Undertake the maintenance and recording of the environmental conditions. Assists with yearly calibration of the equipment.
• Assist with monitoring visits and timely resolution of any related monitoring queries.
• Assist with recording of pharmacy activities for costing purposes on the CT Pharmacy costing trackers, EDGE and resolving costing queries.
What’s in it for You?
At Moorfields, we invest in you—your growth, your wellbeing, your future.
You’ll join a flexible, supportive organisation offering:
• Competitive salary (including high-cost area supplement)
• Membership of the NHS Pension Scheme
• 24/7 independent counselling support
• Career-long learning and development opportunities
• Excellent transport connections
• Access to NHS and Blue Light discount schemes
• Free Pilates classes
• Full support and training to develop your skills
And so much more! To see the full range of benefits we offer please view our Moorfields benefits leaflet.
Clinical Trials:
1. Support the Lead Pharmacy Technician for Clinical trials with the day-to-day management of the pharmacy clinical trials services. Ensure an efficient and consistent service as stipulated in the pharmacy clinical trial Standard Operating Procedures (SOPs) andcurrent legislation governing the management of clinical trials and pharmaceuticals.
2. Support the Lead Pharmacy Technician for Clinical trials in the development and maintenance of the clinical trials services and the production of the relevant trial-specific and Trust-wide clinical trials pharmacy policies.
3. Deputies for Lead Pharmacy Technician for Clinical trials in their absence as appropriate.
4. Assist with the efficient operation of dispensing services within the Clinical Trials. Ensure clinical trial protocols and SOPs are followed at all times and that the Clinical Trials activity trackers are maintained.
5. Ensure the security, recording & maintenance of all Clinical Trial drugs from ordering. receipt, storage, return and destruction.
6. Responsible for ensuring that patient returns are appropriately handled, stored and destroyed, and adequate drug accountability is maintained.
7. Ensure prompt registration to the IWRS for each new trial, and that the IWRS tracker is updated
8. Ensure prompt receipt of shipments and management of temperature excursions according to the trial's specific procedures.
9. Undertake the maintenance and recording of the environmental conditions. Assists with yearly calibration of the equipment.
10.Assist with monitoring visits and timely resolution of any related monitoring queries.
11.Assist with the audit and maintenance of pharmacy Clinical Trial site files, including both electronic and paper records. Ensure that files contain all required documents and comply with current guidelines and legislation.
12.Assist with completion of delegation and training logs as required.
13.Participate in any necessary meetings for Clinical Trials with trial investigators, sponsors, co-coordinators, clinical research associates and any other interested parties.
14.Assist the Clinical Trials pharmacists and pharmacy technicians in setup of Clinical Trials. Produce trial-specific pharmacy guide procedures, accountability logs and labels as appropriate.
15.Assist with protocol amendments and update of pharmacy guides as appropriate.
16.Assist in the ‘closing down’ of completed trials and maintaining archive records.
17.Assist with recording of pharmacy activities for costing purposes on the CT Pharmacy costing trackers, EDGE and resolving costing queries.
Supervisory and training responsibilities:
1. Provide day-to-day supervision, support, and training to rotational pharmacists, pharmacy technicians and pharmacy Assistant Technical Officers (ATOs).
2. Assist with training assessments for Pharmacy staff working within the Clinical Trials section.
Education and Training
1. Act as a role model and provide E&T support on Clinical Trials medicines and processes for new members of staff and those rotating within the Clinical Trials Section.
2. Undertake Continuing Professional Development (CPD) as required by the General Pharmaceutical Council (GPhC).
3. To contribute to the training of other members of the multidisciplinary team within the Trust as required.
4. Develop and motivate staff to ensure they can and do perform well in their job, contribute towards improvements to the pharmaceutical service and encourage staff to suggest and implement changes to improve pharmaceutical services.
Staff Management
1. Assist in the supervision of all aspects of work by junior staff within the Pharmacy Clinical Trials section to ensure that procedures are carried out according to local policy and with due regard to the GPhC standards of conduct, ethics and performance.
2. Assist Lead Clinical Trials Pharmacy Technician in supervision, management and prioritisation of the work processes within the section to ensure adequate staff cover is in place at all times in order to maintain an efficient service.
3. To encourage an open attitude to performance and ensure a no-blame culture to enable review of past performance and implement change.
Professional:
1. Assist with ensuring that appropriate levels of service are provided in accordance with statutory requirements and professional standards, in accordance with the code of ethics by the General Pharmaceutical Council (GPhC) and the professional guide by the Royal Pharmaceutical Society of Great Britain (RPS).
2. Assist with monitoring of compliance with all relevant legislation and associated advice, including the Human Medicines Regulations, the UK Medicines for Human Use and the UK Medicines for Human Use (Clinical Trials), Health and Safety at Work Act (including COSHH).
3. Respect the confidentiality of information relating to patients and management and ensure compliance withGeneral Data Protection Regulations.
4. Be a role model and ambassador for the profession within the hospital and at peer meetings.
5. Be accountable for own professional actions, guided by national guidelines, protocols, legislation, hospital formularies, EU directives on Clinical Trial management, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP).
6. Assist with the delivery of audits related to the Pharmacy service and clinical audits to monitor and promote adherence to local and national guidance.
Personal Development:
1. Undertake and participate in the in-house, regional education training programmes and other activities to develop skills as part of a commitment to develop a Continuing Professional Development (CPD) portfolio to meet all requirements of the General Pharmaceutical Council (GPhC).
2. Maintain Trust mandatory training compliance.
3. Maintain a commitment to self-development and undertake further training opportunities as identified through the appraisal and performance monitoring system.
This advert closes on Sunday 1 Feb 2026