SR CRA I

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

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA’s Site Management team is seeking a Senior Clinical Research Associate in Ireland to cover UK & Ireland sites.

Why IQVIA?

Genuine career development opportunities to grow as we grow.

Flexible working to assist work–life balance and professional success.

Well‑being support covering your physical, mental, and financial health.

Awards

2026 "Glassdoor Best Place to Work in the UK" #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)

Brandon Hall Excellence Award for Learning & Development

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
• Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
• May support start‑up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

• Requires at least 3-5 years of on‑site monitoring experience in interventional clinical trials, including Oncology TA.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Ability to establish and maintain effective working relationships with coworkers and clients.
• Full driving license and vehicle required for travel.
• Please note - this position is not eligible for visa sponsorship. Candidates must hold right to work in UK & Ireland.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.