Senior Scientist I, Clinical Trial Safety (fix Term/secondment)

AstraZeneca

Warsaw, Poland
Not specified (considered office-based due to the nature of the role).
Bsc/msc/phd in life science
Minimum two years clinical study experience
Knowledge of ich/gcp guidelines
AstraZeneca is seeking a Senior Scientist I for Clinical Trial Safety, a fixed-term position based in Warsaw, Poland, running from July 2026 to January 2028. The role involves reviewing clinical safety data and ensuring accurate and complete patient data during clinical trials, while contributing to study start-up and quality control processes

Job Summary

  • The role is part of the Trial Safety Review Center (TRISARC) dedicated to ensuring patient data is complete and medically accurate.
  • The Senior Scientist I reviews critical clinical safety data, generates queries, and supports study teams throughout all phases of the clinical trial.
  • This position requires a collaborative team player who can manage multiple tasks with conflicting deadlines while adhering to strict quality standards.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Scientist I for Clinical Trial Safety, a fixed-term position based in Warsaw, Poland, running from July 2026 to January 2028. The role involves reviewing clinical safety data and ensuring accurate and complete patient data during clinical trials, while contributing to study start-up and quality control processes.

Skills & Requirements

Must-have

  • BSc/MSc/PhD in Life Science
  • Minimum two years clinical study experience
  • Knowledge of ICH/GCP Guidelines
  • SAE reporting requirements understanding
  • Patient narrative preparation skills

Nice-to-have

  • Experience with JReview or JMP Clinical tools
  • Ability to develop advanced computer skills
  • Medical writing experience for narratives
  • Cross-functional collaboration on global studies
  • Aggregated data visualization capabilities

Key Requirements

  • Educational degree in Life Science or equivalent
  • Minimum two years experience in clinical studies
  • Proficiency in spoken and written English

Work Rights

Not specified

Tailored Resume

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