Clinical Site Monitor
Mindlance
Job Description Title: Clinical Site Monitor Location: Los Angeles, CA Duration: 6 Months (Possibility of extension) Responsibilities Perform/facilitate time-efficient pre-study initiation process. Orient site personnel to study protocol/procedures. Monitor compliance to FDA Regulations and Client SOP. Manage study site activities through frequent on-site visits and telephone contacts. Position located in Los Angeles, CA area and will manage sites in this area and help region cover Northern and Southern California as needed. Qualifications Direct multi-therapeutic site monitoring experience, including oncology experience. On-site monitoring experience required of multiple protocols in multiple therapeutic areas, including oncology. Please ensure the Therapeutic Areas and the # of studies handled by the candidate is also listed on the resume. Additional Information This job is with one of my pharmaceutical clients. #J-18808-Ljbffr Mindlance
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