Job Title: Clinical Research Nurse (Part-Time, 3 Days/Week)
Location: Bedford, UK
Hours: Part-time, 3 days per week
Salary: Competitive, dependent on experience
About Us:
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.
Role Overview:
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.
Key Responsibilities:
* 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.
Requirements:
* 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.
Desirable:
* Experience in oncology, haematology, or other specialised therapeutic areas.
* Previous involvement in study setup or regulatory submissions.