Clinical Trial Associate

Job Summary

To support clinical studies in a remote full-time capacity, the Clinical Trial Associate will manage administrative tasks, ensure compliance with regulatory standards, and communicate with research staff while maintaining study documentation and data integrity.

Key responsibilities

• Provide comprehensive administrative support for clinical trial operations, ensuring accuracy and completeness of study documentation within the Trial Master File (TMF)
• Monitor adherence to study protocols and regulatory guidelines, proactively identifying compliance gaps to maintain trial integrity
• Coordinate site communications and support day-to-day trial operations, collaborating with cross-functional teams to resolve operational issues

Required qualifications

• Bachelor's degree or equivalent combination of experience, education, and training
• 2+ years of experience at the Sponsor or CRO level, or 5 years at the SMO or site level
• Experience with medical device clinical studies preferred
• Familiarity with clinical development standards and regulatory requirements (GCP, FDA)
• Proficiency with Microsoft Office, particularly strong Excel skills