Lead SACT Trials Pharmacist

Somerset NHS Charity; Bath; On-site; GBP 53,000 - 61,000; Full time

Job summary

A leading NHS charity is seeking a Senior Specialty Manager for Clinical Trials in Bath. The role involves overseeing oncology and haematology clinical trials, ensuring compliance with regulations, and contributing to the development of the clinical trials portfolio. Candidates should possess a Master of Pharmacy and relevant experience in clinical trials, with a focus on patient care and research excellence.

Qualifications

• Registered pharmacist with the General Pharmaceutical Council.
• 1 year pre-registration training and minimum 3 years’ experience.
• GCP trained.

Responsibilities

• Coordinate pharmaceutical aspects of oncology and haematology clinical trials.
• Lead the setup of clinical trials of investigational medicinal products.
• Ensure compliance with clinical trials regulations.

Skills

Clinical Trials

Oncology

Haematology

Pharmaceutical Dispensing

Aseptic Services

Education

Master of Pharmacy (MPharm)

Postgraduate Diploma in Clinical Pharmacy

Job description

Main area: Pharmacy

Grade: Band 8a

Contract: 12 months (Fixed term)

Hours:

• Part time
• Flexible working
• Compressed hours

18.75 hours per week (Please speak to the team to discuss any flexible arrangements you may wish to consider)

Job ref: 427-7069996

Employer: Royal United Hospitals Bath NHS Foundation Trust

Employer type: NHS

Site: Royal United Hospitals Bath

Town: Bath

Salary: £53,755 - £60,504 PA

Salary period: Yearly

Closing date: 08/06/2025 23:59

Band 8a

Job overview

Research and clinical trials are a very important part of the National Health Service. Everyday clinical trials investigating medicines are being run across the country which are working towards new and improved treatments for patients.

The successful candidate will be a hard-working and professional individual who enjoys being part of research. The principal objective of this role is to provide leadership for the oncology & haematology clinical trials and effective oversight directing the safe and timely set up and maintenance of these clinical trials at the trust.

The post holder will build and expand the oncology & haematology clinical trials portfolio whilst ensuring compliance with International Conference on Harmonisation of Good Clinical Practice (ICH GCP), clinical trials regulations, the research governance framework and other relevant guidelines and policies. The post holder will be responsible for the development and approval of oncology and haematology clinical trials prescriptions.

There is a unique opportunity as part of this role to work within the Cancer Services team in the new Dyson Cancer Centre at the RUH, enabling the postholder to enhance their specialist knowledge in this area.

Main duties of the job

• Coordinate all pharmaceutical aspects of oncology and haematology clinical trials across the Trust, and help ensure the provision of a quality pharmaceutical dispensing and aseptic service to patients.
• Comply with specific guidance and regulations relating to clinical trials, such as ICH GCP, Medicines for Human Use (Clinical Trials) Amendment Regulations 2006, Clinical Trials Directive 2001/20/EC, and other relevant guidelines and policies.
• Lead and direct the setup of oncology & haematology clinical trials of investigational medicinal products (CTIMPs), following sponsor provided documents and within agreed timelines.
• Support and develop the Trust Research & Development portfolio.
• Be the delegated Lead Pharmacist for oncology & haematology and radiopharmacy clinical trials.

Working for our organisation

We value everyone’s contribution, support a compassionate, inclusive environment, and promote diversity. We foster a culture of learning, development, and innovation, supporting staff wellbeing with a comprehensive programme. We believe in holistic wellbeing including physical, emotional, spiritual, and financial health.

Detailed job description and main responsibilities

Please find attached a detailed job description, person specification, and further information about this role.

Person specification

Qualifications & Training

• Master of Pharmacy (MPharm) degree or equivalent
• Registered as a pharmacist with the General Pharmaceutical Council
• Postgraduate Diploma in Clinical Pharmacy or equivalent
• 1 year pre-registration training and minimum 3 years’ experience
• Member of Royal Pharmaceutical Society of Great Britain
• GCP trained

Knowledge & Experience

• Supportive involvement in clinical trials
• Understanding of Clinical Trials legislation
• Experience in Oncology/Haematology
• Experience in pharmacy clinical trials department
• Experience in pharmacy aseptics unit
• Knowledge of cancer treatment developments

Employer certification / accreditation badges

You must have appropriate UK professional registration.

This role involves access to vulnerable people and is subject to DBS checks as per legal requirements.

Name: Hilary Arden

Job title: Senior Specialty Manager, Clinical Trials

Email: [e-mail]

Telephone: [phone]