Clinical Research Associate-Freelance

Translational Research in Oncology; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Translational Research in Oncology (TRIO) is seeking an experienced Clinical Research Associate (CRA) or Senior CRA to join the Monitoring Resources team. This is a remote independent contractor role, full-time for one year, with applicants based in the United States and preference for Central or Western regions.

Responsibilities include data verification, performing site visits (pre-study to termination), and ensuring compliance with FDA/ICH-GCP guidelines.

Qualifications

• 3+ years as CRA/monitoring in oncology trials.
• 1+ year monitoring on early-phase trials.
• Experience with solid tumor trials preferred.

Responsibilities

• Perform data verification of source documents.
• Conduct site visits from pre-study to termination.
• Ensure adherence to FDA, ICH-GCP and local regulations.
• Ensure implementation and compliance with FDA, and ICH-GCP guidelines.
• Assist with data validation and query resolution.
• Mentor junior team members as required.
• Ensure completion and collection of regulatory documents.

Skills

Oncology experience

English fluency

Regulatory knowledge

Travel willingness

Education

Bachelor's degree in science

Tools

Clinical trial systems

Job description

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO could be the place for you!

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 (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.

Responsibilities:

• Performing data verification of source documents;


• Conducting site visits, including pre-study, initiation, monitoring, and termination;


• Confirmingadherence 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

Qualifications:

• 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


• Experience monitoring Phase I trialswill be valued.


• Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred;


• 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.

The contract rate and seniority level will be determined based on the applicant’s education, relevant experience, location, knowledge, skills, and abilities, as well as internal equity and market data.

If you are ready to take the next step in your oncology clinical research career and contribute to meaningful cancer research, we would love to hear from you!

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.

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