Remote Part-Time Clinical Research Associate (Imaging)

QT Imaging, Inc.; Petaluma, Northern (CA, KY); Hybrid; USD 35,000 - 55,000; Part time

Job summary

QT Imaging, Inc. is seeking a motivated Clinical Research Associate (CRA) to support clinical studies for its medical imaging technologies.

This part-time, remote position reports to the Director of Clinical Operations and requires coordination with sites, CROs, and internal stakeholders to ensure compliance with GCP and regulatory standards. The ideal candidate has 5+ years of clinical research experience, site monitoring responsibilities, and familiarity with FDA regulations and ISO standards

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• Minimum 5 years of clinical research experience with site monitoring and data query resolution.
• Experience supporting FDA-regulated clinical studies involving medical devices.
• Experience with diagnostic imaging, radiology, women's health studies, or AI-driven tech is a plus.
• Knowledge of GCP, ICH, FDA regs, and ISO standards for medical device trials.
• Experience with EDC and CTMS systems.
• Strong project management, analytical, and communication skills.

Responsibilities

• Support planning, initiation, execution, monitoring, and closeout of clinical studies.
• Coordinate with sites, CROs, and vendors; track enrollment and milestones.
• Maintain TMF and regulatory documents; prepare reports and dashboards.
• Perform remote and on-site monitoring, review data for accuracy and protocol compliance.
• Assist with investigator meetings and cross-functional collaboration.
• Travel periodically for site visits and study meetings.

Skills

Clinical Research

Site Monitoring

GCP

FDA Regulations

Data Management

CTMS

EDC

Project Management

Education

Bachelor’s degree in Life Sciences

Tools

EDC

CTMS

MS Office

Job description

QT Imaging, Inc. is seeking a motivated Clinical Research Associate (CRA) to support clinical studies for its medical imaging technologies.

This part-time, remote position reports to the Director of Clinical Operations and requires coordination with sites, CROs, and internal stakeholders to ensure compliance with GCP and regulatory standards. The ideal candidate has 5+ years of clinical research experience, site monitoring responsibilities, and familiarity with FDA regulations and ISO standards