Clinical Research Associate - Multiple Roles

AstraZeneca

Fully remote
Site activation and performance
Risk-based monitoring
Patient safety and data integrity
AstraZeneca is seeking multiple Clinical Research Associates to support their Biopharma and Oncology teams, focusing on site activation and performance management for clinical trials. The role emphasizes collaboration with investigators, ensuring compliance, and maintaining high-quality standards throughout the clinical trial process

Job Summary

  • Across BioPharma and Oncology, we design and deliver high‑quality, patient‑centric clinical trials that translate deep biology into breakthrough medicines in cardiovascular, renal & metabolism, respiratory & immunology, and cancers where the need is greatest.
  • As a Clinical Research Associate , you will own site activation and performance, direct risk-based monitoring to where it matters most, and safeguard patient safety and data integrity.
  • At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.

Matching Summary

Match Score: 85

AstraZeneca is seeking multiple Clinical Research Associates to support their Biopharma and Oncology teams, focusing on site activation and performance management for clinical trials. The role emphasizes collaboration with investigators, ensuring compliance, and maintaining high-quality standards throughout the clinical trial process.

Skills & Requirements

Must-have

  • site activation and performance
  • risk-based monitoring
  • patient safety and data integrity
  • ICH-GCP and RbQM
  • Source Data Verification (SDV)
  • Case Report Form (CRF) review
  • Serious Adverse Events (SAEs) reporting

Nice-to-have

  • accelerated start-up timelines
  • data-driven decision-making
  • lifelong learning, growth and development
  • flexible, diverse, and inclusive environment

Key Requirements

  • Bachelor’s degree in life science or related field
  • Solid understanding of drug development process
  • Experience in site selection, activation and monitoring
  • Proficiency with CTMS/eTMF
  • Willingness to travel for site monitoring
  • Fluency in written and spoken business-level English

Work Rights

Not specified

Tailored Resume

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