Role overview

Qualifications

A minimum of 2 years of monitoring experience in oncology trials
Completion of a science-related Bachelor’s degree
Excellent knowledge of medical terminology and clinical monitoring process
Strong ICH-GCPs knowledge

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

Key facts

Remote from: Ireland
Freelance
Mid-level (2-5 years)
Research Assistant
English

Hard skills

Clinical Trial Management Systems Clinical Monitoring FDA Regulations Adaptive Clinical Trials

Other skills

Teamwork
Enthusiasm
Personal Integrity
Innovation

About the company

TRIO - Translational Research in Oncology

Research

TRIO is a unique, full-service oncology clinical research organization (CRO) that leverages the strengths of our worldwide network of Investigators, academic leaders, patient advocates and our clinical research team to accelerate drug development. We’ve spent decades conducting oncology trials from inception to completion, focusing on the best research and science to guide the development of innovative and biologically sound therapies. This translational research model allows us to bring targeted concepts into clinics on the most rational development path. We find the shortest course to save lives. We are focused. We care. We deliver.

Company details

Company typeSME

IndustryResearch

Company size201 - 500

Links

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Job description

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-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

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.

Teamwork · Passion · Integrity · Innovation