Clinical Research Nurse

Green Life Science; Bedford; On-site; GBP 80,000 - 100,000; Part time

Job summary

A leading clinical research organisation is seeking a part-time Clinical Research Nurse to coordinate and deliver clinical trials in Bedford. The role involves ensuring patient safety, managing study participants, and maintaining compliance with GCP and trial regulations. Qualified candidates must be Registered Nurses with experience in clinical research and strong communication skills. This position offers flexible hours, working three days per week, with possibilities for additional shifts depending on project needs.

Qualifications

• Registered Nurse with current NMC registration.
• Proven experience in clinical research within relevant settings.
• Strong knowledge of Good Clinical Practice (GCP).

Responsibilities

• Coordinate and deliver clinical research studies accurately.
• Recruit and manage study participants effectively.
• Conduct clinical assessments and maintain documentation.

Skills

Organisational skills

Communication skills

Interpersonal skills

Flexibility

Education

Registered Nurse (NMC) with current registration

Job description

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.