Clinical Research Associate II (Field CRA)

Added
7 days ago
Type
Full time
Salary
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Related skills

monitoring clinical research clinical data management sops regulatory compliance

πŸ“‹ Description

  • Serve as the site manager, ensuring data entry and query resolution within a timely manner, as well
  • Participate in the monitoring functions in a clinical study including site management
  • Monitor, onsite and remotely, ongoing compliance to study protocols and site adherence to global
  • Prepare and participate in presentation of protocols and other study conduct requirements at study
  • Manage device accountability, inventory, and distribution, with responsibilities of device
  • Participate in the distribution, collection and tracking of regulatory documentation to ensure

🎯 Requirements

  • Bachelor's degree required in biological sciences or health-related field (e.g., biology
  • Working knowledge of medical terminology required
  • Familiarity with laws, regulations, standards and guidance governing the conduct of clinical
  • Excellent verbal, written, and interpersonal communication skills
  • Strong organizational and problem-solving skills; keen attention to detail
  • Intermediate level of competence in Word, Excel, PowerPoint or equivalent programs required

🎁 Benefits

  • A collaborative teamwork environment where learning is constant, and performance is rewarded
  • The opportunity to be part of the team that is revolutionizing the treatment of some of the world's
  • Medical, dental, vision, life, AD&D insurance
  • Short and long-term disability insurance
  • 401(k) with employer match
  • Paid parental leave
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