Clinical Research Associate - 12 Month Contract

AstraZeneca

Base: 109,148.80 to 143,257.80; bonus/equity: vari...
Fully remote
Ich-gcp knowledge
Clinical study management
Monitoring study conduct
AstraZeneca is seeking a Clinical Research Associate (CRA) for a 12-month contract, responsible for overseeing clinical studies at assigned sites. The position requires strong knowledge of clinical trial processes, adherence to regulatory standards, and effective communication skills

Job Summary

  • The Clinical Research Associate (CRA) has local responsibility for the delivery of studies at allocated sites and is an active participant in the local study team(s).
  • The CRA prepares, initiates, monitors, and closes assigned sites in clinical studies, following AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations.
  • AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues, with annual base salary ranging from 109,148.80 to 143,257.80.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Clinical Research Associate (CRA) for a 12-month contract, responsible for overseeing clinical studies at assigned sites. The position requires strong knowledge of clinical trial processes, adherence to regulatory standards, and effective communication skills.

Salary

Base: 109,148.80 to 143,257.80; Bonus/Equity: Variable Pay Bonus/Short Term Incentive opportunity and equity-based long-term incentive program (if applicable); Benefits: Contract Benefits Program

Skills & Requirements

Must-have

  • ICH-GCP knowledge
  • Clinical Study Management
  • monitoring study conduct
  • site initiation and closure
  • data query resolution
  • Serious Adverse Events reporting

Nice-to-have

  • risk-based quality management
  • remote collaborators
  • manage change positively
  • efficient process improvement
  • cultural awareness
  • technology impact on projects

Key Requirements

  • Bachelor degree in life science
  • ICH-GCP knowledge
  • basic GMP/GDP knowledge
  • local regulations knowledge
  • drug development process understanding
  • Valid G driving license

Work Rights

Not specified

Tailored Resume

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