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Clinical Research Associate-Freelance

Translational Research in Oncology

Remote · USContract / Full-timeSeen 3w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
No compensation found
Location
Remote · US
Role Type
Research
Schedule
Contract / Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

TRIO is seeking a Clinical Research Associate or Senior Clinical Research Associate for its Monitoring Resources team. This remote independent-contractor opportunity is a one-year contract requiring full-time availability. The role supports oncology clinical trials through site monitoring, data verification, regulatory compliance, and query resolution. Applicants must be based in the United States, with preference for Central or Western regions, and must be legally authorized to work in the country.

Skills & qualifications

RequiredNice to have

Skills

Oncology ResearchClinical Trial MonitoringEarly Phase TrialsMedical TerminologyClinical Monitoring ProcessICH-GCPClinical Trial Information SystemsSolid Tumor TrialsEnglish

Qualifications

3+ Years Oncology Experience as CRA, CRC, or Research Nurse1+ Year Early Phase Trial MonitoringPhase I Trial Monitoring ExperienceBachelor's in Science-Related FieldMust Be Legally Authorized to Work in the United StatesMust Travel Up to 60%

Full 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;

  • 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

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 trials will 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.

Teamwork · Passion · Integrity · Innovation

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How this job compares

Set against the 591 open Clinical Research Associate jobs on Olive Jobs, counted October 31, 2026.

Pay
  • This postingNot listed
  • US median$75–175K/yr242 salary ranges
  • US median$59–65/hr52 hourly ranges
Openings
Olive Jobs lists 30 open Clinical Research Associate jobs in Texas and 591 across the US. 16% of them nationwide are listed as remote or flexible.
Hiring the most in Texas
Experience
This posting asks for at least 3 years of experience; Clinical Research Associate postings that state a minimum ask for 2 years at the median (535 postings).
Education
This posting asks for a bachelor's degree; 127 of the 591 open Clinical Research Associate jobs (21%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on October 31, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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