Clinical Trials/Monitoring Specialist

Job Title: Clinical Trials/Monitoring SpecialistPay Rate: $60 to $63.78/HRDuration: 12 monthsLocation: Anywhere in California (Travel to Clinical sites)We are looking for a Clinical Trials/Monitoring Specialist to field monitor studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, and more.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 client to the field sites and through final disposition.Conduct onsite monitor visitsEducation and Experience:Bachelor's Degree or equivalent in a related field5-7 years of experience required