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Clinical Research Associate

NuvOx Pharma • Tucson, AZ, US • published 2026-10-16 20:20:29.761819

Description

**Position Summary:** The In\-House CRA will support the planning, monitoring, and execution of clinical trials to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. This role will focus on remote and on\-site monitoring activities, including Source Data Verification (SDV), clinical data review, and site support, while also contributing to in\-house clinical operations activities. **Responsibilities:** * Conduct remote and on\-site monitoring activities in accordance with the monitoring plan, ensuring high\-quality data and protocol compliance. * Review eCRFs and source data, resolve discrepancies, and follow up with sites to ensure timely data cleaning and query resolution. * Identify, document, and escalate data quality issues, protocol deviations, and site risks to Clinical Operations leadership. * Perform Investigator Site File (ISF) reviews, tracking and addressing outstanding issues. * Oversee essential document management during all study phases and ensure audit\-readiness Trial Master File (TMF). * Prepare, review, and file monitoring visit reports, follow\-up letters, and study documentation. * Ensure compliance with study pr...

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