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Clinical Monitoring Specialist

REMOTE, CA 00000

Posted: 11/21/2025 Employment Type: Contract Job Category: Clinical Development and Operations Job Number: 624000 Is job remote?: Yes Country: United States

Job Description

Target PR Range: 50-60/hr
*Depending on experience

Summary:
The main function of a clinical monitoring specialist is to field monitor studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts and more.

Key Responsibilities:
• Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g. Contracts), and recommend and develop process improvements.
• Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded.
• Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.
• Conduct onsite monitor visits

Education and Experience:
• Bachelor's Degree or equivalent in related field
• 5-7 years of experience required

*CO/NYC candidates might not be considered
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