Part Time jobs in United Kingdom

• Coordinate and deliver clinical research studies in accordance with protocol, Good Clinical Practice (GCP), and relevant regulations.
• Recruit, consent, and manage study participants, providing ongoing support and education.
• Conduct clinical assessments, sample collection, and data recording accurately and efficiently.
• Liaise with principal investigators, study teams, and external stakeholders to ensure smooth trial operations.
• Maintain accurate and up-to-date documentation, including source records, case report forms, and regulatory files.
• Monitor patient safety and report adverse events promptly.
• Contribute to continuous improvement initiatives and participate in training as required.

We are seeking an experienced and motivated Clinical Research Nurse to join our Bedford team on a part-time basis. You will play a key role in the planning, coordination, and delivery of clinical trials, ensuring patient safety, data integrity, and regulatory compliance. Registered Nurse (NMC) with current registration.

• Proven experience in clinical research, ideally within hospital or community‑based research settings.
• Strong knowledge of GCP and clinical trial regulations.
• Excellent organisational, communication, and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Flexibility to work three days per week, with occasional additional hours if required.

• Experience in oncology, haematology, or other specialised therapeutic areas.
• Previous involvement in study setup or regulatory submissions.

We are a leading clinical research organisation committed to advancing patient care through high‑quality clinical trials. We work across a variety of therapeutic areas, providing patients with access to cutting‑edge treatments while ensuring rigorous compliance with all research standards.