Job Description
Position Title: Clinical Research Monitoring, Senior Specialist
Work Location: Sacramento, CA, 94203
Assignment Duration: 12 Months
Work Arrangement: Field-based (requires onsite monitoring visits)
Position 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 the organization to the field sites and through final disposition.
• Conduct onsite monitor visits
Qualification & Experience:
• Bachelor's Degree or equivalent in related field
• 5-7 years of experience required
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 58.22/hr.