Clinical Research Associate II - North Carolina

Added
11 days ago
Type
Full time
Salary
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Related skills

crm gcp clinical trials site monitoring ich-gcp

πŸ“‹ Description

  • Advance AbbVie's pipeline by striving for excellence in clinical research
  • Partners with investigator/site staff for meaningful engagements
  • Focus on site trials to ensure conduct, data integrity, and patient safety
  • Primary contact for investigative sites; provide context on trials and connect stakeholders
  • Train and motivate site staff and investigators on trial goals and patient treatment principles
  • Monitor site activities for protocol compliance, GCPs, and quality standards

🎯 Requirements

  • Relevant tertiary qualification in health-related disciplines preferred
  • Minimum 1 year clinically related experience; 6 months in clinical research monitoring
  • Knowledge of regulatory requirements, ICH/GCP, and applicable policies
  • Strong cross-functional collaboration, planning, and organizational skills
  • Ability to leverage technology and CRM tools to support site engagement
  • Excellent interpersonal, communication, and presentation abilities

🎁 Benefits

  • Comprehensive benefits package including medical/dental/vision insurance
  • Paid time off (vacation/holidays/sick)
  • 401(k) plan and eligibility for short-term incentive programs
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