UK CRA – Sponsor-Dedicated, On-Site Monitoring

IQVIA Inc; Reading; Vor Ort; GBP 32.000 - 46.000; Vollzeit

Zusammenfassung

IQVIA is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring, ensure GCP/ICH compliance, and drive site recruitment plans. The role involves regular site visits, training, and close collaboration with the study team across diverse sites.

Candidates should have independent monitoring experience, strong GCP/ICH knowledge, and flexibility to travel. This is a sponsor-dedicated CRA position based in the UK.

Qualifikationen

• Experience of independent on-site monitoring (minimum 6 months).
• Manage multiple clinical trial protocols across diverse sites.
• In-depth knowledge of GCP and ICH guidelines.

Aufgaben

• Perform site monitoring visits in accordance with GCP/ICH guidelines.
• Work with sites to drive and track recruitment plans to align with project needs.
• Administer protocol training to sites and establish regular communication.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Track submissions, recruitment, CRF completion and data queries; may support start-up.
• Maintain TMF/ISF documents and ensure regulatory filing readiness.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team members for project execution support.

Kenntnisse

On-site monitoring

Clinical trial management

GCP & ICH knowledge

Travel flexibility

Ausbildung

Life science degree

Jobbeschreibung

IQVIA is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring, ensure GCP/ICH compliance, and drive site recruitment plans. The role involves regular site visits, training, and close collaboration with the study team across diverse sites.

Candidates should have independent monitoring experience, strong GCP/ICH knowledge, and flexibility to travel. This is a sponsor-dedicated CRA position based in the UK.