Clinical Research Practitioner-SACT coordinator

🔒 Confidential Employer
Posted 3 May 2026
LOCATION
Southampton
TYPE
Full-time
LEVEL
Mid-Senior level
SALARY
£39,043 / year
CATEGORY
Healthcare
This employer holds a UK Home Office sponsor license — sponsorship for this specific role is at the employer’s discretion

SKILLS

Clinical Research SACT coordination Communication Organizational Skills Time Management IT Skills Team-working Patient Care

FULL DESCRIPTION

Clinical Research Practitioner-SACT coordinator

Band 5 - Permanent - Part time 30 hours per week - [Employer hidden — view at passion-project.co.uk] - Southampton General Hospital - Salary £32,073 - £39,043 per annum pro rata - Closing 13/05/2026

Job overview

[Employer hidden] is delighted to offer a fantastic opportunity to work with us. Please see below for detailed job description of the role.

Main duties of the job

We strive to ensure that research is considered as a treatment option for all eligible participants, and we work closely with clinical teams and within patient clinical pathways to ensure that research opportunities are met. We are pleased to offer an exciting opportunity within the Cancer Research Team for a motivated and enthusiastic Band 5 Clinical Research Practitioner (CRP). As a key member of the research workforce, you will work collaboratively with the cancer research delivery teams, Senior Research Nursing team, Pharmacy, Research Education team, and a wide range of clinical and non-clinical colleagues to support the safe and effective delivery of trial related research medications. This includes Systemic Anti-Cancer Therapies (SACT), alongside the delivery of high-quality research across the cancer research portfolio. The Cancer Research Team is involved in both early and late phase clinical studies and manages a diverse range of trial medications that are delivered in conjunction with routine clinical care. This is a newly developed role, designed to enhance the coordination and timely provision of trial medications. The primary focus of the post is to ensure that research participants receive their trial treatments efficiently, safely, and in alignment with their research journey, supporting excellent patient experience and trial delivery.

Working for our organisation

University Hospital Southampton is one of England's largest acute teaching Trusts, offering a wide range of learning and development opportunities to support your career aspirations. Located on the south coast with an international airport and direct rail links to London, Southampton offers an ideal setting to live and work, with the New Forest, South Downs and Jurassic Coast. We believe that using technology wisely shows strong time management and commitment to innovation. However, personalizing your recruitment application to highlight your unique skills and experiences is crucial. Relying too heavily on generic, AI-generated content instead of drawing from your own strengths and accomplishments may lead to your application being rejected if multiple candidates present identical or similar information. At UHS we’re committed to providing a flexible working environment where possible. Whether you are balancing family, study, or your wellbeing with your career, we want to support you so you can help our patients. At UHS, we proudly champion individuality, recognizing that outstanding care is only possible with a diverse, inclusive team. We’re committed to creating an anti-racist, anti-discriminatory environment where everyone feels valued, safe, and empowered to make a meaningful impact in our communities. We welcome applicants of all backgrounds, identities, and experiences to join us in building a healthcare community where everyone can belong, thrive, and contribute.

Detailed job description and main responsibilities

As a Band 5 CRP, you will demonstrate the ability to work independently and use initiative, supported by excellent organisational and communication skills. You will contribute to the effective management and coordination of all trial medications and act as a key point of contact for research participants throughout their trial pathway. The successful candidate will have substantial experience at Band 4 within a clinical research setting and will be confident in communicating clearly, calmly, and professionally with all members of the multidisciplinary research team. You will play a vital role in facilitating effective communication across teams to support high-quality research delivery and participant experience. Following a robust induction, the successful candidate will be able to:

  • Communicate effectively with all those involved in the research SACT pathway to ensure that research SACT treatments are available at the scheduled time and that patients have the best possible experience. A point of contact for research patients and /or representatives regarding the preparation of their treatment.
  • Provide specialist research and clinical care to research participants.
  • Assist in the management, coordination and implementation of research programmes.
We are looking for an enthusiastic individual who is organised, self-motivated and aspires to further their career in clinical research. You will have experience of clinical research and can work in a fast-paced clinical environment and demonstrate the ability to prioritise and deliver agreed objectives within specific time frames. Team-working skills, flexibility and drive will be required to ensure the success of this post. You will need to have an excellent level of written and verbal communication skills, with IT skills being essential. You will work in collaboration with a multidisciplinary team.

Person specification

Qualifications, knowledge and experience

Essential criteria:
Degree or equivalent in Life, Physiological or Physical Sciences or related field or able to demonstrate clearly equivalent level of theoretical and practical knowledge
Recent NHS clinical research experience or equivalent
Evidence of on-going professional development
Significant clinical experience, working face to face with patients, in a relevant speciality with proven ability and competence to undertake a range of clinical tasks, including but not limited to, vital signs, body measurements, personal care.
Understanding of personal accountability
Conversant in relevant safeguarding policies
Able to understand complex/scientific/medical terminology
Willingness to work towards level of skills and competencies required in line with accreditation for Clinical Research Practitioners through the Academy of Health care Sciences

Desirable criteria:
Specialist qualification/registration
International Conference on Harmonisation/Good Clinical Practice (ICH/GCP) Certification
Provide evidence of teaching and supporting learners in practice
Knowledge of UK Policy Framework for Health & Social Care, International Conference on Harmonisation/Good Clinical Practice (ICH/GCP)
Experience with NHS IT systems (eCamis, Charts, EDMS).

Skills

Essential criteria:
Communication
Organisational skills
Time management
Attention to detail
Taking the initiative
General IT skills
Working under pressure
Interpersonal skills
Multitasking
Analytical thinking

Trust Values

Essential criteria:
Patients First
Always Improving
Working Together

Please be advised that this vacancy may close earlier than stated if we receive a large number of applications. We will not accept any applications or queries via agencies, under any circumstances. For more information about our Trust, visit https://careers.uhs.nhs.uk. Getting to work - our travel promise: ...

Further details / informal visits contact

Name: Emma Gaunt
Job title: Senior Research Sister
Email: [contact hidden]
Telephone: [contact hidden]

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