CRA II (UK/Ireland) – Phase 3b/4 Monitoring

IQVIA; Dublin; On-site; EUR 45,000 - 60,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across therapeutic areas. The CRA will cover sites across the UK & Ireland, performing initiation, monitoring and close-out visits in accordance with GCP/ICH guidelines.

This role involves coordinating with sites to drive subject recruitment and ensuring high-quality data collection. Ideal candidates have 1–2 years of on-site monitoring experience, a life-sciences degree, and strong knowledge of regulatory

Qualifications

• 1–2 years of on-site monitoring experience.
• Degree in scientific discipline or health care or equivalent.
• Good knowledge of GCP and ICH guidelines.
• Ability to establish and maintain effective working relationships with coworkers and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per GCP/ICH and contracted scope.
• Drive and track subject recruitment plans to support project timelines.
• Administer protocol training and establish regular communication with sites.
• Evaluate site practices and escalate quality issues as needed.
• Manage study progress: regulatory submissions, recruitment, CRF completion, data queries; may assist start-up.
• Ensure TMF/ISF documents are complete and filed per regulatory requirements.
• Document site management activities and submit visit reports and follow-up communication.
• Collaborate with study team members for project execution.

Skills

On-site monitoring

Regulatory knowledge

Stakeholder management

Communication

Education

Bachelor's degree in life sciences

Job description

IQVIA is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across therapeutic areas. The CRA will cover sites across the UK & Ireland, performing initiation, monitoring and close-out visits in accordance with GCP/ICH guidelines.

This role involves coordinating with sites to drive subject recruitment and ensuring high-quality data collection. Ideal candidates have 1–2 years of on-site monitoring experience, a life-sciences degree, and strong knowledge of regulatory