Clinical Site Manager

  • Location
    Irvine, California
  • Job type
    Contract/Temporary
  • Category
    Medical & Science - Pharmaceutical - Clinical

A Clinical Site Manager job in Irvine, CA is available through Adecco Medical and Science. You will responsible for executing study start-up for assigned protocols with the goal of meeting study start-up timeliness. You will have a bachelor’s in life sciences or related field. Monitor project plans to meet Site Initiation Readiness at the Investigator Meeting.


Clinical Site Manager job responsibilities include:
• Maintain project metrics and provide status updates to senior management.
• Execute study start-up for assigned protocols within company timelines by identifying clinical team needs, contracting and managing vendor supported tasks and tracking critical timelines.
• Monitor project plans and communicates and troubleshoots the leading and lagging indicators to meet Site Initiation Readiness at the Investigator Meeting.


Maintain the tracking of project metrics in Site Start-Up tracker and provide status updates.
• Site Regulatory Documents Collection (FDA Form 1572, Signature Pages, Medical Licenses, etc.)

QUALIFICATIONS:

• Qualified candidates will have a bachelor’s in life sciences or related field
• At least 2 years experience in clinical research
• Prefer candidate with prior experience as Study Start-Up Specialist but not mandatory.
• Knowledge of FDA regulations required.

If you are interested in this Clinical Site Manager job in Irvine, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to www.adeccousa.com.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled



  • Apply with Adecco

Reference number US_EN_2_108175_322336