Clinical Research Associate

Added
6 days ago
Type
Full time
Salary
Salary not provided

Related skills

crm gcp data integrity site monitoring risk-based monitoring
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๐Ÿ“‹ Description

  • Primary contact for investigative site and engage sites effectively
  • Aligns, trains, and motivates site staff and PI on trial goals
  • Conducts site evaluation, training, monitoring per protocol and SOPs
  • Develops site engagement strategies using CRM tools
  • Connects protocol and patient journey to trial execution
  • Mentor junior CRAs and participate in initiatives

๐ŸŽฏ Requirements

  • Tertiary qualification in health-related field preferred
  • 1+ year clinical research monitoring experience (6 months in trials)
  • Knowledge of regulatory requirements, ICH/GCP
  • Strong cross-functional collaboration and planning skills
  • Ability to leverage technology for site-centric support
  • Excellent communication and stakeholder management

๐ŸŽ Benefits

  • AbbVie equality and opportunity employer information
  • US & Puerto Rico accommodation info links provided
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