Clinical Research Associate - Rare Disease

AstraZeneca

Fully remote
Ich-gcp guidelines
Local regulations knowledge
Clinical study monitoring
The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s)

Job Summary

  • The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s).
  • This role involves the selection, initiation, monitoring, and closure of assigned sites in clinical studies, adhering to AstraZeneca Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations.
  • At AstraZeneca, we push the boundaries of science to transform complex biology into transformative medicines for rare diseases.

Matching Summary

The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s).

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • local regulations knowledge
  • clinical study monitoring
  • site selection and initiation
  • essential document management
  • remote and onsite monitoring visits

Nice-to-have

  • work in matrix reporting structure
  • manage change positively
  • champion efficient processes
  • prioritize multiple tasks
  • proactive and assertive communication
  • experience in rare medical conditions

Key Requirements

  • Bachelor’s degree or equivalent
  • Experience of monitoring
  • Excellent knowledge of ICH-GCP
  • Good knowledge of local regulations
  • Willingness to travel up to 70%

Work Rights

Not specified

Tailored Resume

Cover Letter