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Onsite Clinical Site Monitor - Oncology (LA)

Mindlance, Inc.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at 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 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. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply #J-18808-Ljbffr Mindlance, Inc.

Vacancy posted 1 day ago
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