Clinical Research Associate
Location
Ireland
Posted
6 days ago
Salary
0
Seniority
Mid Level
No structured requirement data.
Job Description
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.
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