Clinical Site Monitor

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.