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Clinical Research Associate 1 - CFSP

IQVIA · Lisbon, Portugal

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks a Clinical Research Associate for site-based clinical trial monitoring in Lisbon. The role involves conducting site visits, managing study progress, and ensuring regulatory compliance throughout the clinical research process.

What they're looking for

  • University degree in scientific or healthcare discipline
  • Minimum 1 year of on-site clinical trial monitoring experience
  • Proficient in Microsoft Office and standard computer applications
  • Fluent in Portuguese and English languages
  • Strong organizational and problem-solving abilities
  • Valid class B driver's license
  • Willingness to travel regularly

What you'll be doing

  • Conduct site selection, initiation, monitoring, and closeout visits
  • Develop and support subject recruitment planning activities
  • Assess site compliance with GCP and ICH guidelines and regulatory requirements
  • Track study progress including submissions, enrollment, and data query resolution
  • Collaborate with site personnel and client representatives on study execution

Privacy & handoff

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What RoleLantern checked

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RoleLantern checkedNeeds clarity
Date posted4 days ago
Last source checkToday
Salary listedNeeds clarity
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