Study Start Up Manager

AstraZeneca

Barcelona, Spain
Ich-gcp compliance
Clinical study start-up
Regulatory document delivery
As a Study Start Up Manager, you will turn complex regulatory and operational requirements into a predictable, high-quality path to site activation

Job Summary

  • As a Study Start Up Manager, you will turn complex regulatory and operational requirements into a predictable, high-quality path to site activation.
  • Your work will directly reduce start-up bottlenecks and help advance multiple indications across a diverse portfolio, supporting our goal to bring several novel therapies forward.
  • Working within the local Study Delivery Team and partnering closely with Contracts, Feasibility and Study Support Services in US SM&M, you will connect strategy with execution, use data to inform decisions, and align stakeholders around clear activation milestones.

Matching Summary

As a Study Start Up Manager, you will turn complex regulatory and operational requirements into a predictable, high-quality path to site activation.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • Clinical study start-up
  • Regulatory document delivery
  • Site activation
  • Veeva Clinical Vault usage

Nice-to-have

  • Cross-functional collaboration
  • Data-driven decision making
  • Stakeholder alignment
  • Proactive risk identification

Key Requirements

  • Bachelor's degree in relevant discipline
  • Experience in Study Management
  • Knowledge of Clinical Development legislation

Work Rights

Not specified

Tailored Resume

Cover Letter