Clinical Site Monitor

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com. 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 contracts •    Position located in Los Angeles, CA area and will manage sites in this area and help region cover Northern and Southern California as needed. Requirements: •    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. •    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. This Job is with one of my pharmaceutical client.