Clinical Research Associate-Freelance

Translational Research in Oncology • Dallas, TX

1d • $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) or Senior Clinical Research Associate (Senior CRA) to join our Monitoring Resources team. This is a remote Independent Contractor opportunity under a one-year contract requiring full-time availability. Applicants must be based in the United States, with preference given to candidates located in the Central or Western regions.

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
• Assisting with data validation and query resolution
• Mentoring junior team members as required
• Ensuring the completion and collection of regulatory documents

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level