Lead, Clinical Research Associate - Arizona

Added
2 days ago
Type
Full time
Salary
Salary not provided

Related skills

people management gcp site visits ctms trial master file

๐Ÿ“‹ Description

  • Lead CRA to oversee monitoring and site management in trials.
  • Must live within a couple hours of Tempe, AZ location.
  • Direct supervision of CRA staff and contractors.
  • Hire, onboard and train staff with HR support.
  • Allocate staff to projects and monitor workload.
  • May act as CRA for selected studies.

๐ŸŽฏ Requirements

  • Bachelor's degree in biomedical or life sciences.
  • 5+ years in clinical operations with 3+ years onsite monitoring.
  • People management skills.
  • Excellent English communication (oral and written).
  • Knowledge of GCP, 21 CFR Part 11, and regulatory requirements.
  • Independent and team-oriented, self-motivated.

๐ŸŽ Benefits

  • Celerion values: Integrity, Trust, Teamwork, Respect
  • Equal Opportunity Employer
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