Clinical Research Associate – Cell Therapy

AstraZeneca

Tennessee, US
Base: $112,154.40 - $168,231.60; bonus/equity: sho...
Fully remote
Bachelor's degree in life sciences
Minimum 3 years cra experience
Ich-gcp guidelines knowledge
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies ensuring compliance with AstraZeneca Procedural Documents and ICH-GCP guidelines

Job Summary

  • The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies ensuring compliance with AstraZeneca Procedural Documents and ICH-GCP guidelines.
  • This field-based position requires strong collaboration with local study teams to drive site performance, resolve issues proactively, and maintain inspection-ready Investigator Site Files.
  • Candidates will benefit from an inclusive culture that champions diversity, offers a competitive base pay ranging from $112,154.40 to $168,231.60, and provides comprehensive health and retirement benefits.

Matching Summary

The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies ensuring compliance with AstraZeneca Procedural Documents and ICH-GCP guidelines.

Salary

Base: $112,154.40 - $168,231.60; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: 401(k), paid vacation, holidays, medical, dental, vision coverage

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences
  • Minimum 3 years CRA experience
  • ICH-GCP guidelines knowledge
  • Site initiation and monitoring
  • Source Data Verification (SDV)
  • Risk Based Quality Management (RbQM)

Nice-to-have

  • Cell Therapy clinical trial experience
  • Remote monitoring proficiency
  • Process improvement mindset
  • Cross-functional collaboration skills
  • Adaptability to change management

Key Requirements

  • Bachelor's degree in Life Sciences or equivalent
  • 3+ years of CRA experience in pharma/biotech/CRO
  • Strong knowledge of ICH-GCP and local regulations
  • Ability to travel nationally and internationally

Work Rights

Not specified

Tailored Resume

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