Senior Analyst I, Clinical Trial Safety

AstraZeneca

Durham, NC, US
3d onsite
Clinical trial safety data analysis
Data review tool set-up and maintenance
Programming experience in data analysis
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe

Job Summary

  • At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.
  • The Senior Analyst I, Clinical Trial Safety is responsible for tools set-up, scripting, and data analysis tasks for the Clinical Trial Safety and works closely with Analysts and Scientists to ensure safety data deliverables meet quality and timelines.
  • AstraZeneca is an equal opportunity employer committed to diversity, inclusion, and providing accommodations for persons with disabilities throughout the recruitment process.

Matching Summary

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.

Skills & Requirements

Must-have

  • Clinical Trial Safety data analysis
  • Data Review tool set-up and maintenance
  • Programming experience in data analysis
  • Knowledge of ICH/GCP Guidelines
  • SAE reporting requirements
  • Advanced Microsoft Excel skills
  • Hybrid work policy with onsite presence

Nice-to-have

  • Cross-functional collaboration
  • Clinical data visualization
  • Experience with JReview or Spotfire
  • Strong attention to detail
  • Statistical knowledge
  • Continuous improvement mindset

Key Requirements

  • Bachelor degree in related discipline
  • Minimum 2 years clinical study experience
  • Understanding of clinical study and drug development
  • Proven organizational and analytical skills
  • Excellent English communication skills

Work Rights

Not specified

Tailored Resume

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