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CRA II Dublin

Fortrea


Job Location:

Dublin - Ireland

Monthly Salary: Not provided by the employer
Posted: 14 August 2026 (30+ days ago)
Application Deadline: 11 November 2026
Vacancies: 1 Vacancy

Job Summary

Fortrea is hiring an experienced CRA II to join our client-dedicated team supporting a leading global pharmaceutical company. This is a home-based role in Ireland with a preference for candidates located in the Dublin area.

Why Join Fortrea
  • Be part of a global innovative organization driving advancements in clinical research.
  • Work in a dedicated partnership with a leading pharmaceutical sponsor.
  • Contribute to Phase II and III interventional clinical trials across a range of therapeutic areas.
  • Enjoy career growth opportunities ongoing development and exposure to high-impact studies.
  • Join a collaborative and supportive team that values quality accountability and innovation.
Key Responsibilities
  • Conduct and oversee study site monitoring visits to ensure compliance with protocols GCP regulatory requirements and company SOPs.
  • Manage all aspects of site activities including site initiation routine monitoring visits and closeout visits.
  • Ensure patient safety data integrity and inspection readiness throughout the study lifecycle.
  • Support site feasibility investigator engagement and collaboration with study stakeholders.
  • Report and follow up on Serious Adverse Events (SAEs) and other safety-related issues as required.
  • Maintain accurate documentation and timely communication with sites and project teams.
  • Demonstrate a proactive approach to problem-solving and issue resolution.
What Were Looking For
  • University/college degree in life sciences or a related healthcare field.
  • Previous experience as a Clinical Research Associate or in a comparable clinical research role.
  • Experience supporting Phase II and/or Phase III interventional drug studies preferred.
  • Experience in Oncology is advantageous.
  • Strong understanding of ICH-GCP regulatory requirements and clinical trial processes.
  • Excellent written and verbal communication skills.
  • Strong collaboration and stakeholder management abilities.
  • Comfortable working across multiple systems and technologies including adapting to new and evolving processes and tools.
  • Valid drivers license and willingness to travel within Ireland.

Join Fortrea and help bring innovative therapies to patients while advancing your career within a global clinical research organization!

Learn more about our EEO & Accommodations request here.


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