Clinical Research Associate

Trzdev35

Experience in study management
Knowledge of clinical development
Document management skills
The role ensures the delivery of a centrally managed study management service across clinical studies from start-up to reporting

Job Summary

  • The role ensures the delivery of a centrally managed study management service across clinical studies from start-up to reporting.
  • The Clinical Research Associate serves as the main contact for document management until the Clinical Study Report is finalized.
  • This position involves liaising with compliance teams to enhance regulatory processes and improve methodologies.

Matching Summary

The role ensures the delivery of a centrally managed study management service across clinical studies from start-up to reporting.

Skills & Requirements

Must-have

  • Experience in Study Management
  • Knowledge of Clinical Development
  • Document Management skills

Nice-to-have

  • Understanding of regulatory processes
  • Ability to improve methodologies
  • Up-to-date with industry best practices

Key Requirements

  • Bachelor’s degree in relevant discipline
  • Experience within a pharmaceutical background
  • Knowledge of relevant legislation

Work Rights

Not specified

Tailored Resume

Cover Letter