Clinical Research Associate — Specialized CRO, London

RBW Consulting; Greater London; Sur place; GBP 42 000 - 60 000; Plein temps

Résumé du poste

RBW Consulting in London seeks a Clinical Research Associate to join a specialist CRO environment. You will monitor studies, ensure compliance with GCP, and support site management with investigators and staff.

The role offers focused work within a scientific organisation, closer mentorship, and opportunities to develop expertise in clinical research processes, documentation, and study delivery.

Qualifications

• Previous clinical trial monitoring experience is essential.
• Experience may include independent monitoring or shadow monitoring.
• Exposure to clinical research within a CRO, sponsor, NHS research, academic research, healthcare, or clinical trials environment.
• Strong organisational skills and attention to detail.
• Excellent communication skills and a collaborative approach.
• Ability to work from the London office as required and on site visits.

Responsabilités

• Perform monitoring activities across clinical research studies.
• Support site management and study conduct in line with protocol, GCP, and regulatory requirements.
• Build and maintain strong relationships with investigators and site staff.
• Ensure study documentation is accurate, complete, and inspection-ready.
• Work closely with clinical operations and scientific teams to support study delivery.

Connaissances

Clinical trial monitoring

GCP knowledge

Regulatory compliance

Communication skills

Organisational skills

On-site coordination

Description du poste

RBW Consulting in London seeks a Clinical Research Associate to join a specialist CRO environment. You will monitor studies, ensure compliance with GCP, and support site management with investigators and staff.

The role offers focused work within a scientific organisation, closer mentorship, and opportunities to develop expertise in clinical research processes, documentation, and study delivery.