Clinical Research Associate

AstraZeneca

Us
Base: $112,154.40 - $168,231.60; bonus/equity: sho...
Fully remote
Ich-gcp compliance
Site monitoring
Data query resolution
The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations

Job Summary

  • The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations.
  • At AstraZeneca we’re dedicated to being a Great Place to Work.
  • Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage.

Matching Summary

The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations.

Salary

Base: $112,154.40 - $168,231.60; Bonus/Equity: short-term incentive bonus opportunity, equity-based long-term incentive program (salaried roles), commission payment eligibility (sales roles); Benefits: qualified retirement program [401(k) plan], paid vacation and holidays, paid leaves, health benefits

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • site monitoring
  • data query resolution
  • Serious Adverse Events reporting
  • essential document management

Nice-to-have

  • change management
  • risk-based monitoring
  • cultural awareness
  • technology adoption

Key Requirements

  • Bachelor's degree in related discipline
  • 3+ years of relevant experience
  • Knowledge of ICH-GCP
  • Ability to travel

Work Rights

Not specified

Tailored Resume

Cover Letter