Clinical Research Nurse

Actalent; Orpington; On-site; GBP 30,000 - 41,000; Full time

Job summary

Actalent is seeking a Clinical Research Nurse for a 6-month contract in Bromley. This role focuses on clinical research coordination, patient management and study administration, rather than invasive procedures.

You will be responsible for coordinating visits, supporting consent, and maintaining documentation while ensuring GCP compliance. The ideal candidate is a registered nurse with NMC registration, strong organisational and communication skills, and experience in clinical trials or research

Qualifications

• Registered Nurse with current NMC registration.
• Experience in clinical trials or a research environment.
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Excellent communication and patient-facing skills.
• Ability to work independently and manage competing priorities.

Responsibilities

• Support delivery and coordination of clinical research studies and trials.
• Identify and screen potential participants for research studies.
• Coordinate patient appointments and study visits.
• Support the informed consent process.
• Maintain accurate study records and research documentation.
• Collect and enter study data in accordance with study protocols.
• Liaise with investigators, sponsors, clinicians and patients.
• Ensure compliance with GCP, regulatory requirements and study protocols.
• Support preparation for monitoring visits, audits and inspections.
• Track study progress and assist with reporting activities.

Skills

Registered Nurse

GCP certification

Patient management

Study coordination

Data entry

Tools

Electronic patient records

Research databases

Job description

Clinical Research Nurse – 6-Month Contract

Location: Bromley

Contract Type: 6-month contract

Hours: Full-time

About the Role

We are looking for a Clinical Research Nurse to join one of our clients, a leading global clinical research organisation.

This position is primarily focused on clinical research coordination, patient management and study administration, rather than invasive clinical procedures. It would suit a registered nurse who is highly organised, confident working with patients and interested in developing or continuing a career within clinical research.

Key Responsibilities

• Support the delivery and coordination of clinical research studies and trials.
• Identify and screen potential participants for research studies.
• Coordinate patient appointments and study visits.
• Support the informed consent process.
• Maintain accurate study records and research documentation.
• Collect and enter study data in accordance with study protocols.
• Liaise with investigators, sponsors, clinicians and patients.
• Ensure compliance with Good Clinical Practice (GCP), regulatory requirements and study protocols.
• Support preparation for monitoring visits, audits and inspections.
• Track study progress and assist with reporting activities.
• Registered Nurse with current NMC registration.
• Strong administrative and organisational skills.
• Excellent communication and patient-facing skills.
• Ability to work independently and manage competing priorities.
• High level of accuracy and attention to detail.
• Previous experience within clinical trials or a research environment.
• Good Clinical Practice (GCP) certification.
• Knowledge of oncology pathways and treatments.
• Experience using electronic patient records and research databases.