Clinical Research Associate II - North Carolina

Added
4 days ago
Type
Full time
Salary
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Related skills

crm gcp site monitoring sops ich-gcp

πŸ“‹ Description

  • Primary contact for investigative sites; support site engagement
  • Aligns and trains site staff on trial goals and patient care
  • Monitors site activities per protocol, GCPs, and SOPs
  • Customizes site engagement strategy using CRM data
  • Connects protocol to day-to-day trial execution and recruitment plans
  • Mentors less experienced CRAs and may join task forces

🎯 Requirements

  • Health-related degree or equivalent preferred
  • 1+ year clinical research monitoring exp; RBM familiarity
  • Therapeutic area knowledge preferred
  • Strong regulatory knowledge (ICH/GCP) and policies
  • Cross-functional collaboration and planning skills
  • Excellent communication and site relationship abilities

🎁 Benefits

  • Comprehensive benefits package ( PTO, medical/dental/vision, 401(k))
  • Eligible for short-term incentive programs
  • Equal opportunity employer commitment
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