Job summary The James Paget Hospital Pharmacy Team is looking for an enthusiastic, highly motivated Pharmacy Technician to join our Clinical Trials team and contribute to our growing service. The Pharmacy department is a diverse and inclusive team. This advert is for a vacancy for 15.5 hours per week, hours of work will be confirmed between the successful applicant and the line manager. We will consider applications for existing Pharmacy staff to undertake this role in conjunction with their current role in line with our service requirements. Our vision is to provide safe, high quality seamless services delivered with courtesy and respect. The Pharmacy team work one in every six weekends to support our 7-day service. We are looking for a qualified technician to join our clinical trials pharmacy team, providing support with the management of the Trust portfolio of clinical trials. Main duties of the job To act as a member of the pharmacy team, undertaking a full range of duties commensurate with the professional role of a pharmacy technician, under the supervision of the Chief Pharmacist whilst working within the legal requirements, Trust policies and department procedures as laid down by the department and the Trust. Main duties for this role will include supporting the pharmacist after set up of a new clinical trial to maintain the medication, training logs and standard operating procedures. The post holder will be responsible for overseeing monitoring visits, maintaining files, close out visits and achieving. The service will be developing to include medicines reconciliation of new patients recruited to clinical trials. To work flexibly, responding to the needs of the department which will include participating in the weekend rota, bank holiday rota and late clinic rota. About us Our vibrant team consists of approximately 90 highly skilled staff who work together to empower our patients to use medicines safely and effectively to improve their health outcomes. The successful candidate will benefit from drawing on the knowledge and experience of approachable staff so you will feel supported and mentored throughout your learning journey. We pride ourselves on creating a positive, supportive and structured learning environment enabling you to strive for success. All roles within the trust require staff to demonstrate our core values and behaviours in the care they provide to patients. All members of staff should consider these behaviours and essential part of their job role. COLLABORATION - We work positively with others to achieve shared aims. ACCOUNTABILITY - We act with professionalism and integrity, delivering what we commit to, embedding learning when things do not go to plan. RESPECT - We are anti-discriminatory, treating people fairly and creating a sense of belonging and pride. EMPOWERMENT - We speak out when things don't feel right, we are innovative and make changes to support continuous improvement. SUPPORT - We are compassionate, listen attentively and are kind to ourselves and each other. Date posted 06 February 2025 Pay scheme Agenda for change Band Band 5 Salary £29,970 to £36,483 a year per annum, pro rata Contract Permanent Working pattern Part-time, Flexible working Reference number 177-EMER-6905309 Job locations James Paget University Hospital Lowestoft Road Gorleston, Great Yarmouth NR31 6LA Job description Job responsibilities Main responsibilities of the role are: 1. To co-ordinate, supervise and maintain the Pharmacy clinical trials service in accordance with ICH GCP guidelines and Pharmacy procedures and ensure provision of a high quality service to patients and staff within the Trust.2. To attend set up meetings, working closely with Clinical Research Associates and Research Nurses and identifying issues and negotiating to ensure resolution.3. To assist with preparing and maintaining dispensing and prescribing guidelines/ procedures for clinical trials within the Trust.4. To be responsible for ensuring that all trial specific procedures are in place in time for the recruitment of the first patient to a new clinical trial.5. To be responsible for the controlled storage of all drugs, including CDs, licensed and unlicensed drugs, and materials sourced or supplied by sponsors for use in clinical trial studies in line with GMP and the Medicines Act 1968.6. To ensure dispensing, storage and expiry date records for clinical trials are kept up-to-date and archived for future reference.7. To be responsible for the ordering and receipt of pharmaceuticals and sundries required to support clinical trial work.8. To be responsible for monitoring stock levels of clinical trial supplies and expiry date checks and take required action in the event of stock discrepancies where necessary.9. To be responsible for accurate record keeping and drug accountability of clinical trials.10. To be responsible for the accountability of all investigational medicinal products returns/disposed medicines according to GCP and GMP.11. To organise the dispensing, preparation and recording of clinical trial products.12. To provide and co-ordinate the training of all Pharmacy staff in clinical trials with regard to trial set up, day-to-day trial queries and monitoring their progress and ICH GCP dispensing practice.13. To be responsible for the closing of completed trials and maintaining archive records.14. To be familiar with procedures and activities of other internal sections within Pharmacy and their potential interactions with trial activities.15. To undertake the counselling of patients on the correct use of clinical trial medication/devices.16. To deputise for the Clinical Trials Pharmacist, when required.17. To undertake a programme of audit to demonstrate adherence to local and national guidelines and legislation in relation to R&D activity. Job description Job responsibilities Main responsibilities of the role are: 1. To co-ordinate, supervise and maintain the Pharmacy clinical trials service in accordance with ICH GCP guidelines and Pharmacy procedures and ensure provision of a high quality service to patients and staff within the Trust.2. To attend set up meetings, working closely with Clinical Research Associates and Research Nurses and identifying issues and negotiating to ensure resolution.3. To assist with preparing and maintaining dispensing and prescribing guidelines/ procedures for clinical trials within the Trust.4. To be responsible for ensuring that all trial specific procedures are in place in time for the recruitment of the first patient to a new clinical trial.5. To be responsible for the controlled storage of all drugs, including CDs, licensed and unlicensed drugs, and materials sourced or supplied by sponsors for use in clinical trial studies in line with GMP and the Medicines Act 1968.6. To ensure dispensing, storage and expiry date records for clinical trials are kept up-to-date and archived for future reference.7. To be responsible for the ordering and receipt of pharmaceuticals and sundries required to support clinical trial work.8. To be responsible for monitoring stock levels of clinical trial supplies and expiry date checks and take required action in the event of stock discrepancies where necessary.9. To be responsible for accurate record keeping and drug accountability of clinical trials.10. To be responsible for the accountability of all investigational medicinal products returns/disposed medicines according to GCP and GMP.11. To organise the dispensing, preparation and recording of clinical trial products.12. To provide and co-ordinate the training of all Pharmacy staff in clinical trials with regard to trial set up, day-to-day trial queries and monitoring their progress and ICH GCP dispensing practice.13. To be responsible for the closing of completed trials and maintaining archive records.14. To be familiar with procedures and activities of other internal sections within Pharmacy and their potential interactions with trial activities.15. To undertake the counselling of patients on the correct use of clinical trial medication/devices.16. To deputise for the Clinical Trials Pharmacist, when required.17. To undertake a programme of audit to demonstrate adherence to local and national guidelines and legislation in relation to R&D activity. Person Specification Education and Qualifications Essential NVQ Level 3 or equivalent Registration with General Pharmaceutical Council Accredited Checking Technician Desirable Patient counselling training Accredited Medicine Management Technician Skills and Experience Essential Post-qualification experience within hospital. Able to work under pressure Understanding of GCP Desirable Significant experience in the set-up and running of a clinical trial in a pharmacy environment Significant experience in pharmacy clinical trials Basic understanding of GMP Experience in aseptic services Skills and Competencies Essential Articulate and numerate Methodical approach to work procedures Excellent oral and written communication skills with ability to demonstrate fluency, clarity and effectiveness. Able to record information accurately with attention to detail Ability to identify and manage problems Able to meet deadlines Trust Values and Behaviours Essential Courteous and Respectful Kind and Helpful Responsive Communication Effective and Professional Person Specification Education and Qualifications Essential NVQ Level 3 or equivalent Registration with General Pharmaceutical Council Accredited Checking Technician Desirable Patient counselling training Accredited Medicine Management Technician Skills and Experience Essential Post-qualification experience within hospital. Able to work under pressure Understanding of GCP Desirable Significant experience in the set-up and running of a clinical trial in a pharmacy environment Significant experience in pharmacy clinical trials Basic understanding of GMP Experience in aseptic services Skills and Competencies Essential Articulate and numerate Methodical approach to work procedures Excellent oral and written communication skills with ability to demonstrate fluency, clarity and effectiveness. Able to record information accurately with attention to detail Ability to identify and manage problems Able to meet deadlines Trust Values and Behaviours Essential Courteous and Respectful Kind and Helpful Responsive Communication Effective and Professional Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Additional information Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Employer details Employer name James Paget University Hospitals NHS Foundation Trust Address James Paget University Hospital Lowestoft Road Gorleston, Great Yarmouth NR31 6LA Employer's website https://www.jpaget.nhs.uk/work-for-us/ (Opens in a new tab)