Clinical Research Nurse – Trials Coordinator (6-Month)

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

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