Study Start Up Manager

AstraZeneca

Barcelona, Spain
Fluency in english and spanish required
Ich-gcp compliance knowledge
Veeva clinical vault experience
This role is based in Barcelona with a requirement to work on-site three days per week

Job Summary

  • This role is based in Barcelona with a requirement to work on-site three days per week.
  • The Study Start Up Manager will accelerate site activation to ensure patients access groundbreaking cancer trials sooner.
  • You will be responsible for obtaining essential documentation, managing regulatory binders, and ensuring compliance with ICH-GCP standards.

Matching Summary

This role is based in Barcelona with a requirement to work on-site three days per week.

Skills & Requirements

Must-have

  • Fluency in English and Spanish required
  • ICH-GCP compliance knowledge
  • Veeva Clinical Vault experience
  • Site activation coordination
  • Regulatory document management

Nice-to-have

  • Advanced degree in relevant field
  • Professional certification in study management
  • Cross-functional stakeholder alignment
  • Data-driven decision making skills
  • Experience with oncology trials

Key Requirements

  • Bachelor's degree in relevant discipline
  • Experience in Study Management within pharmaceutical or clinical background
  • Knowledge of clinical development legislation

Work Rights

Not specified

Tailored Resume

Cover Letter