Clinical Research Associate - Rare Disease

AstraZeneca

Cotia, Brazil
Fully remote
Ich-gcp guidelines knowledge
Local regulations knowledge
Monitoring clinical studies
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.
  • AstraZeneca pushes 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 knowledge
  • local regulations knowledge
  • monitoring clinical studies
  • site selection and initiation
  • remote and onsite monitoring visits
  • essential document management

Nice-to-have

  • work in matrix reporting structure
  • champion more efficient methods
  • proactivity and assertiveness
  • understand technology impact
  • experience in rare medical conditions

Key Requirements

  • Bachelor's degree in life science
  • demonstrated monitoring experience
  • basic knowledge of GMP/GDP
  • good medical knowledge
  • drug development process understanding
  • clinical study management understanding
  • attention to details
  • written and verbal communication skills
  • collaboration and interpersonal skills
  • negotiation skills
  • flexibility in schedule and travel

Work Rights

Not specified

Tailored Resume

Cover Letter