SR CRA I

IQVIA; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Research Associate to cover UK & Ireland sites from Ireland. You will perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH, manage site communications and ensure protocol adherence throughout the study.

The role requires 3–5 years of on-site monitoring experience in interventional trials (oncology preferred), strong regulatory knowledge, and a valid driving license for travel.

Qualifications

• 3–5 years of on-site monitoring experience in interventional clinical trials (oncology a plus).
• Strong knowledge of GCP/ICH and regulatory requirements.
• Ability to establish effective working relationships with sites and study teams.
• Willingness to travel as required; valid driving license.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) in accordance with GCP/ICH and contracted scope.
• Drive recruitment and retention strategies at site level to support study timelines.
• Train site staff on protocol requirements and ensure regular communication of study updates.
• Assess site practices for protocol adherence and quality, escalating issues as needed.
• Track regulatory submissions, approvals, recruitment, CRF completion and data queries; support start-up as needed.
• Maintain TMF/ISF documentation and generate visit reports and follow-up letters.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory compliance

Stakeholder management

Driving license

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.

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.