Senior Clinical Research Associate

Added
24 hours ago
Type
Full time
Salary
Salary not provided

Related skills

gcp data quality clinical trials site monitoring ich
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๐Ÿ“‹ Description

  • Serve as primary Sponsor contact for investigative sites
  • Train and motivate site staff and PI on trial goals
  • Conduct site evaluation, training, monitoring, and closure
  • Develop site engagement strategy and track progress
  • Link protocol and science to day-to-day trial activities
  • Support recruitment and protocol compliance

๐ŸŽฏ Requirements

  • Health discipline degree (preferred)
  • 3+ years in clinical research monitoring
  • Familiar with risk-based monitoring (RBM)
  • Strong knowledge of ICH/GCP and local regulations
  • Excellent communication and cross-functional collaboration
  • Ability to plan, organize, and manage multiple projects

๐ŸŽ Benefits

  • Flexible work arrangements in a matrixed global environment
  • Dedicated learning, development and leadership opportunities
  • Commitment to diversity and inclusion
  • Code of conduct and integrity emphasis
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