Senior Clinical Research Associate - UK & Ireland

IQVIA; Dublin; On-site; EUR 65,000 - 95,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Research Associate to cover UK & Ireland sites, with on-site monitoring across Ireland and travel to UK/IE locations. The role focuses on ensuring protocol compliance, regulatory adherence, and high-quality data in interventional oncology trials.

You will lead site interactions, deliver protocol training, and manage recruitment plans while maintaining TMF/ISF documentation and timely study reporting.

Qualifications

• 3–5 years of on-site monitoring in interventional trials (Oncology).
• Strong knowledge of GCP/ICH and regulatory requirements.
• Excellent site relationships and travel readiness.

Responsibilities

• Perform site monitoring visits per scope and GCP/ICH guidelines.
• Drive subject recruitment plans aligned with project needs.
• Provide protocol training and maintain regular site communications.
• Assess site practices for protocol conduct and regulatory adherence.
• Track regulatory submissions, enrollments, CRFs, and data queries.
• Maintain TMF/ISF and generate visit reports with follow-ups.

Skills

On-site monitoring

GCP/ICH knowledge

Stakeholder communication

Travel willingness

Clinical trial coordination

Education

Bachelor's degree in Life Sciences

Tools

EDC (e.g., Medidata)

TMF systems

Job description

IQVIA is seeking a Senior Clinical Research Associate to cover UK & Ireland sites, with on-site monitoring across Ireland and travel to UK/IE locations. The role focuses on ensuring protocol compliance, regulatory adherence, and high-quality data in interventional oncology trials.

You will lead site interactions, deliver protocol training, and manage recruitment plans while maintaining TMF/ISF documentation and timely study reporting.