Clinical Research Associate

Added
8 hours ago
Type
Full time
Salary
Salary not provided

Related skills

crm gcp recruitment site monitoring ich guidelines

๐Ÿ“‹ Description

  • Primary contact for investigative site; engage with sites and stakeholders
  • Aligns and trains site staff and PI on trial goals and patient treatment
  • Conducts site evaluation, training, monitoring per protocol and plans
  • Customize site engagement strategy per assigned study
  • Utilizes CRM to report progress and measure impact
  • Connect protocol and scientific principles to trial execution

๐ŸŽฏ Requirements

  • Health-related degree preferred
  • Minimum 1 year clinically related experience; 6 months in clinical research monitoring
  • Familiar with risk-based monitoring; onsite and offsite monitoring
  • Knowledge of therapeutic areas and clinical trial concepts
  • ICH/GCP guidelines and local regulatory requirements
  • Strong cross-functional collaboration and organizational skills

๐ŸŽ Benefits

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