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Site Start Up Specialist
MEIRxRS / Med Exec Intl
 
Job Location: Irvine, CA
Education/Experience
  • BS in life sciences or related field
  • At least 2 years experience in clinical research
  • Knowledge of FDA regulations
  • Prior Study Start-Up experience preferred
  • Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook
  • Experience with Adobe Acrobat Professional and Microsoft Access a plus
  • Presentation Delivery

Responsibilities
  • Execute study start-up for assigned protocols within company timelines by identifying clinical team needs,
  • Oversee Site Start-Up project budgets
  • Review and report on deliverables of vendors
  • Maintain the tracking of project metrics in Site Start-Up tracker and provide status updates
  • Manage information sharing
  • Develop Standard Operating Procedures and Working Documents to document and communicate unit’s processes and procedures
  • Schedule and lead site start-up meetings with clinical team and vendors to review any issues, items for escalation, regulatory document issues, and IRB status
  • Set and meet personal and professional goals and objectives




How To Apply:
You will be directed to another website for application instructions.
 
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