Clinical Site Monitor

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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.

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 client.