[Hiring] Clinical Research Associate @Translational Research in Oncology

Role Description

TRIO is looking for a Clinical Research Associate to join our Monitoring Resource team. Reporting to the CRA Line Manager, this position will be a remote full-time freelance position based in Ireland.

• Performing data verification of source documents;
• Conducting site visits, including pre-study, initiation, monitoring, and termination;
• Confirming adherence to all FDA, ICH-GCP, and local regulations;
• Ensuring implementation and compliance with FDA, and ICH-GCP guidelines;
• Participating in budget negotiation and follow-up where applicable;
• Assisting with data validation and query resolution;
• Mentoring junior team members as required;
• Ensuring the completion and collection of regulatory documents.

Qualifications

• A minimum of 2 years of monitoring experience in oncology trials;
• Experience monitoring in early-phase trials will be valued;
• Completion of a science-related Bachelor’s degree;
• Excellent knowledge of medical terminology and clinical monitoring process;
• Strong ICH-GCPs knowledge;
• Experience with clinical trial information systems;
• Ability to travel up to 60% on average;
• Must be legally authorized to work in the country.

Requirements

• Prior to applying please review TRIO's Applicant Information Notice;
• To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI;
• To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI-generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.

Benefits

• Teamwork;
• Passion;
• Integrity;
• Innovation.