Clinical Research Associate

Added
less than a minute ago
Type
Full time
Salary
Salary not provided

Related skills

gcp clinical research site monitoring ich guidelines regulatory compliance
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📋 Description

  • Hybrid CRA role in Amadora, Portugal
  • Partner with investigators and site staff for study delivery
  • Ensure quality conduct and patient safety across Phase I–IV
  • Coordinate site qualification, initiation, monitoring, and close-out visits
  • Train site personnel on protocol and safety reporting
  • Oversee risks, CAPA plans, and regulatory compliance

🎯 Requirements

  • Bachelor’s degree in health/science or related field preferred
  • Minimum one year in clinical research monitoring
  • Strong planning, organizational, and communication skills
  • Analytical, problem-solving, and ability to manage multiple priorities
  • Self-motivated, collaborative, committed to quality and patient safety

🎁 Benefits

  • AbbVie culture and values: All4OneAbbVie, Decide Smart & Sure, Agile & Accountable
  • Equal Opportunity Employer; focus on integrity, innovation and collaboration
  • US & Puerto Rico resources for accommodations and support
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