Research Nurse/Trial Practitioner

HCA Healthcare UK; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

An established industry player is seeking a Clinical Research Nurse/Clinical Trial Practitioner to join their world-leading clinical trials facility in London. This role involves planning and implementing expert research care, ensuring compliance with Good Clinical Practice, and supporting patient recruitment for groundbreaking oncology trials. With a commitment to providing the latest treatments and a supportive work environment, this position offers excellent career progression opportunities. Join a team that values kindness, honesty, and integrity, and contribute to the development of new therapies for cancer patients.

Benefits

25 days holiday plus bank holidays

Private Healthcare Insurance

Private pension contributions

Season Ticket Loan

Cycle to Work scheme

Group Life Assurance

Critical Illness Cover

Enhanced Maternity and Paternity pay

Staff discounts

Flexible benefits

Qualifications

• At least 3 years of research and trial coordination experience.
• Experience in early-phase clinical trials and oncology.

Responsibilities

• Plan and evaluate expert research care for clinical trial patients.
• Ensure compliance with Good Clinical Practice standards.
• Coordinate and manage a portfolio of translational clinical research.

Skills

Patient assessment

Phlebotomy skills

Research coordination

Oncology Trials experience

Good Clinical Practice (GCP)

Education

Current NMC registration

Job description

Clinical Research Nurse/Clinical Trial Practitioner
London: Sarah Cannon Research Institute/ Private Care @ Guys (Satellite Site)
Working Hours: Full time: 37.5 hrs per week (Monday – Friday, 9 am - 5 pm)
Contract Type: Fixed Term Contract
Salary: Competitive (DOE) plus Benefits

About the role

We’re seeking a Clinical Research Nurse/Clinical Trial Practitioner to join Sarah Cannon Research Institute (SCRI), rated “Good” by the CQC. Flexibility to work at our London Bridge Satellite site is required.

SCRI is a world-leading clinical trials facility specializing in developing new therapies, including targeted and precision medications for cancer patients.

Responsibilities

1. Plan, implement, and evaluate expert research care; support patients enrolled in clinical trials.
2. Ensure research complies with Good Clinical Practice (GCP) standards, safeguarding patient well-being.
3. Develop strong relationships with study investigators to ensure patient safety.
4. Support patient recruitment and oversee high-quality early-phase clinical studies.
5. Work flexibly across teams to ensure smooth operation of the research facility.
6. Act as the patient's key worker, providing support and assistance.
7. Coordinate and manage a portfolio of translational clinical research.
8. Supervise and monitor side effects of drugs and treatments used in trials.

Qualifications

Must have:

• Current NMC registration (if a Registered Nurse)
• At least 3 years of research and trial coordination experience, including early-phase trials
• Experience in Oncology Trials or Clinical Trials
• Patient assessment and phlebotomy skills

Why join us?

HCA UK, founded over 50 years ago, is one of the world’s leading healthcare providers. We invest heavily in the latest treatments and facilities, providing excellent opportunities for career progression and a supportive working environment.

Benefits include:

• 25 days holiday plus bank holidays, with options to buy or sell leave
• Private Healthcare Insurance
• Private pension contributions
• Season Ticket Loan and Cycle to Work scheme
• Group Life Assurance, Critical Illness Cover
• Enhanced Maternity and Paternity pay
• Staff discounts and flexible benefits

Our values

We value kindness, honesty, integrity, and respect. We are committed to creating an inclusive environment where everyone can bring their full selves to work.

Additional information

We offer reasonable adjustments and flexible working arrangements to support all candidates.

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