Study Delivery Sr Associate

Amgen UK

Master's degree or equivalent clinical experience
Experience with ctms, etmf, and edc systems
Global clinical trial execution oversight
The role provides essential global study management support to ensure timely, high-quality, and compliant study execution

Job Summary

  • The role provides essential global study management support to ensure timely, high-quality, and compliant study execution.
  • Candidates will partner with Study Managers to deliver start-up activities, manage risk monitoring, and escalate early warning signals.
  • The position involves maintaining clinical trial systems like CTMS and ensuring inspection readiness through proper documentation management.

Matching Summary

The role provides essential global study management support to ensure timely, high-quality, and compliant study execution.

Skills & Requirements

Must-have

  • Master's degree or equivalent clinical experience
  • Experience with CTMS, eTMF, and EDC systems
  • Global clinical trial execution oversight
  • Vendor management and supplier coordination
  • Risk-based monitoring and CAPA implementation

Nice-to-have

  • Strong collaborative communication skills
  • Proactive issue identification and escalation
  • Process improvement and automation mindset
  • Cultural sensitivity for global team collaboration
  • Curiosity and willingness to learn new tasks

Key Requirements

  • Master's degree OR Bachelor's + 2 years experience
  • 1 year biopharmaceutical clinical research experience
  • Experience working on global clinical trials
  • Knowledge of regulatory compliance and audit processes

Work Rights

Not specified

Tailored Resume

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