Clinical Research Associate

Added
18 minutes ago
Type
Full time
Salary
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Related skills

gcp clinical research site monitoring ich guidelines sops

📋 Description

  • Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into
  • Partners with the investigator and site staff for meaningful and effective engagements positioning
  • Focus on site clinical research that ensures appropriate conduct of the trial while driving

🎯 Requirements

  • Appropriate tertiary qualification, health related preferred (e.g., Medical, Scientific, Nursing).
  • Minimum of 1 year clinically-related experience, with 6 months in clinical research monitoring
  • On-site monitoring experience in investigational drug or device trials required.
  • Knowledge of therapeutic indications relevant to clinical trials.
  • Regulations governing clinical research, ICH/GCP Guidelines, and applicable regulations.
  • Strong planning, organizational, analytical, and communication skills with the ability to handle
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