Clinical Research Practitioner-SACT coordinator
Location
Southampton, England, United Kingdom
Employment TypeFull-time
Posted At5/9/2026
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (46.0%).
Occupation TypeBusiness associate professionals not elsewhere classified.
Occupation Code Skill LevelMedium Skilled
Sponsorship Salary Threshold
£41,700
(£21.38 per hour)
Standard minimum applies
Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.
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Description
Job Overview
University Hospital Southampton NHS Foundation Trust 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
University Hospital Southampton NHS Foundation Trust 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
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:
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
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.
- Provide specialist research and clinical care to research participants.
- Assist in the management, coordination and implementation of research programmes.
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
Essential criteria
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
- 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).
Essential criteria
- Communication
- Organisational skills
- Time management
- Attention to detail
- Taking the initiative
- General IT skills
- Working under pressure
- Interpersonal skills
- Multitasking
- Analytical thinking
Essential criteria
- Patients First
- Always Improving
- Working Together