Clinical Research Associate

Translational Research in Oncology•Dallas, TX

2d•$95,000 - $120,000•Remote

About The Position

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. TRIO is looking for a Clinical Research Associate (CRA) to join our Monitoring Resources team. This is a full-time, remote position for candidates based in the Central and Western United States and will require travel to clinical trial sites.

Requirements

A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse
Minimum of 1 year monitoring experience on an early phase trial
Fluent in English
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 United States

Nice To Haves

Experience monitoring phase I trials will be valued
Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred

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