Clinical Research Associate

GT Medical Technologies, Inc.

Clinical Research Associate conducting monitoring activities for clinical studies across various sites. Ensuring compliance with GCP, regulatory standards, and study protocols while managing data accuracy.

Posted 4/28/2026full-timeRemote • Arizona • 🇺🇸 United StatesJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct site monitoring visits, including site feasibility, initiation, routine monitoring, and close-out visits, in accordance with SOP, protocol requirements, GCP and applicable regulatory requirements.
Deliver protocol-specific and study-related training to assigned sites and maintain consistent communication to address study expectations, questions, and emerging issues.
Perform source data review and verification to ensure accuracy and completeness of clinical trial data.
Assess site compliance with the protocol, GCP, and applicable regulations by reviewing study conduct, documentation practices, and data quality; escalate significant findings when necessary.
Monitor overall study progress at assigned sites by reviewing enrollment activity, CRF completion, EDC entry, and query resolution.
Escalate site compliance issues, protocol deviations, and data quality concerns to the CRM/Senior CRM as appropriate.
Verify that essential regulatory documents are collected and filed appropriately in the Trial Master File (TMF) and confirm that the Investigator Site File (ISF) is maintained in accordance with GCP and local regulatory standards.
Document monitoring activities and site interactions through timely visit reports, follow-up correspondence, and action plans to ensure resolution of findings.
Collaborate with cross-functional study team members to support effective study execution and issue resolution.
Contribute to the development and implementation of site-level recruitment plans when applicable.
Conduct site close-out visits and ensure resolution of outstanding data queries, regulatory reconciliation, and completion of required site close-out activities.
Provide support during site start-up activities as needed.
Support regulatory document management activities, including tracking, and filing of required study documentation.

Requirements

What you’ll need

Bachelor’s degree in a scientific or health-related discipline preferred.
Minimum of 2 years of related experience in clinical research required.
Experience as a Clinical Research Coordinator(CRC) or Sponsor CRA required.
Experience with clinical site data collection and/or monitoring required.
GCP training and certification required.
Oncology clinical research experience strongly preferred.
Working knowledge of computer systems and standard business applications.
Strong verbal and written communication skills.
Excellent organizational skills along with strong attention to detail and accuracy.
Ability to work independently while also collaborating effectively with cross-functional teams.
Proficiency in Microsoft office applications (SharePoint, Word, Excel and PowerPoint).
Flexibility to work varied schedules as needed.
Satisfactorily pass comprehensive background screening.

Benefits

Comp & perks

50% travel required for work, events, and training.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial data reviewsource data verificationsite monitoringprotocol compliance assessmentdata quality monitoringregulatory document managementrecruitment plan developmentclinical site data collectionGCP trainingclinical research experience

Soft Skills

strong verbal communicationstrong written communicationexcellent organizational skillsattention to detailindependent workcollaborationproblem-solvingflexibilitytime managementissue resolution

Certifications

GCP certification