Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.
Our passionate team is committed to providing cancer treatments of the future to the world of today.
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.
Responsibilities
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-GCP knowledge
Experience with clinical trial information systems
Ability to travel up to 60% on average
Must be legally authorized to work in the country
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