Clinical Research Nurse

Barrington James; Aberdeen City; On-site; GBP 80,000 - 100,000; Full time

Job summary

A healthcare organization based in Aberdeen is seeking a Clinical Research Nurse. This role involves the safe delivery of clinical research studies in accordance with Good Clinical Practice (GCP) and regulatory requirements. The candidate will coordinate study visits, ensure patient advocacy, and contribute to research quality improvement initiatives. A valid NMC registration, degree-level qualification, and experience in clinical research are essential. The position offers opportunities for ongoing professional development and flexibility in working hours.

Benefits

Ongoing professional development

Research training support

Qualifications

• Knowledge of clinical research and Good Clinical Practice (GCP).
• Valid GCP certification.
• Experience working with electronic data capture systems.

Responsibilities

• Deliver clinical research studies in line with approved protocols and GCP.
• Coordinate study visits and liaise with clinical departments.
• Act as a patient advocate, ensuring participants are informed and supported.

Skills

Excellent communication and interpersonal skills

Strong organisational skills with attention to detail

Ability to work independently and as part of a multidisciplinary team

Education

Registered Nurse (Adult) with valid NMC registration

Degree-level qualification or equivalent clinical experience

Job description

Clinical Research / Research & Development

Reports to

Job Purpose

The Clinical Research Nurse will be responsible for the safe and effective delivery of clinical research studies in accordance with Good Clinical Practice (GCP), regulatory requirements.iso, and local policies. The post holder will work collaboratively with investigators, research teams, and clinical services to support the set-up, conduct, and close-out of clinical trials and research studies.

Key Responsibilities

Clinical Research Delivery

• Deliver clinical research studies in line with approvedaundry protocols, GCP, and ethical approvals
• Screen, recruit, consent, and follow up research participants
• Perform study-related clinical procedures (e.g., observations, venepuncture, ECGs, sample processing)
• Monitor participant safety and report adverse events in accordance with regulatory requirements

Study Management

• Coordinate study visits and liaise with clinical departments to ensure smooth study delivery
• Maintain accurate and contemporaneous study documentation, including case report forms and source data
• Assist with study set-up, site initiation, monitoring visits, and close-out activities
• Support data collection, query resolution, and audit readiness

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Participant Care and Advocacy

• Act as a patient advocate, ensuring participants are fully informed and supported throughout their research journey
• Provide clear information to participants and respond to questions or concerns
• Ensure confidentiality and data protection standards are upheld at all times

Collaboration and Communication

• Work closely with Principal Investigators, sponsors, CROs, and multidisciplinary teams
• Communicate effectively with clinical staff, research teams, and external stakeholders
• Contribute to team meetings, service development, and quality improvement initiatives

Governance and Compliance

• Ensure compliance with GCP, GDPR, MHRA regulations, and local SOPs
• Support inspections and audits as required
• Maintain mandatory training and professional registration

Person Specification

• Registered Nurse (Adult) with valid NMC registration
• Degree-level qualification or equivalent clinical experience
• Knowledge of clinical research and Good Clinical Practice (GCP)
• Excellent communication and interpersonal skills
• Strong organisational skills with attention to detail
• Ability to work independently and as part of a multidisciplinary team
• Previous experience in a clinical research or research-active environment
• Valid GCP certification
• Experience in informed consent and clinical trial documentation
• Knowledge of regulatory and ethical frameworks for clinical research
• Experience working with electronic data capture systems

Additional Information

• The post may involve working across multiple clinical areas within Aberdeen
• Some flexibility in working hours may be required to meet study needs
• Ongoing professional development and research training will be supported

Clinical Research Nurse • Aberdeen, Scotland, United Kingdom