Clinical Research Assistant

Job Title

Clinical Research Assistant

Location

Van Nuys, CA (In-Person)

Company Overview

EosDx is revolutionizing early cancer detection through compact bio-crystallography hardware and AI-enabled diagnostics. Our mission is to make cancer detection painless, accurate, and accessible — starting with a non-invasive breast exam designed to save lives, reduce healthcare costs, and eliminate unnecessary anxiety.

Role Summary

EosDx is seeking a Clinical Research Assistant (CRA) to support ongoing and upcoming clinical studies evaluating our diagnostic technology. The CRA will assist with study coordination, data collection, regulatory documentation, and participant management. This position offers a hands-on opportunity to contribute directly to research that has the potential to transform how cancer is detected and managed.

Key Responsibilities

• Support the planning, execution, and monitoring of clinical research studies in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Assist with participant recruitment, screening, scheduling, and obtaining informed consent.
• Prepare and maintain accurate and organized study records, logs, and case report forms (CRFs).
• Collect and manage clinical and technical data from study participants and sites.
• Coordinate with clinical sites, investigators, and cross-functional EosDx teams to ensure smooth study operations.
• Assist in preparing study materials including protocols, informed consent forms, and regulatory submissions.
• Support Institutional Review Board (IRB) communications, submissions, and amendments.
• Monitor data quality, resolve discrepancies, and support preparation of reports and summaries.
• Maintain compliance with all ethical, legal, and company standards in clinical research activities.
• Interact professionally with study participants to ensure comfort, safety, and confidentiality throughout the study process.

Qualifications

• Bachelor’s degree in life sciences, biomedical engineering, public health, or a related field.
• 0–3 years of experience in a clinical research, laboratory, or healthcare environment (internship or academic research experience acceptable).
• Strong attention to detail, documentation accuracy, and data management skills.
• Excellent communication, organizational, and interpersonal abilities.
• Ability to work both independently and collaboratively in a fast-paced clinical setting.
• Passion for advancing healthcare innovation and improving patient outcomes.

Preferred Attributes

• Experience working in medical device, diagnostics, or imaging research.
• Prior experience supporting IRB submissions, study documentation, or data management.
• Familiarity with clinical research regulations (GCP, FDA, IRB processes) preferred.
• Proficiency with clinical data management systems or EDC platforms.
• Interest in women’s health and early cancer detection.

Compensation

Salary will be determined based on experience and qualifications.
EosDx offers a competitive compensation package that includes base salary, health coverage, paid time off, and opportunities for professional growth within a mission-driven team.

Reporting & Team Structure

• Reports to: Chief Medical Officer and Clinical Supervisor.
• Works closely with hardware, software, and data science teams to coordinate study activities.
• Interfaces directly with clinical investigators, research coordinators, and study participants.

Job Type: Full-time

Pay: $25.00 - $30.00 per hour

Work Location: In person