Regional Clinical Trial Management Associate

BeiGene

Market competitive compensation; performance-based...
Fluent in english listening and writing
2 years clinical or drug development experience
Bs in relevant scientific discipline preferred
This role supports the execution of clinical trials with a focus on quality standards and administrative efficiency within a global oncology company

Job Summary

  • This role supports the execution of clinical trials with a focus on quality standards and administrative efficiency within a global oncology company.
  • The position involves managing Trial Master Files, assisting with vendor registration, and supporting local regulatory submissions including SUSAR reports.
  • BeOne offers a competitive compensation package with performance bonuses, company shares, and opportunities for professional development in a dynamic team.

Matching Summary

This role supports the execution of clinical trials with a focus on quality standards and administrative efficiency within a global oncology company.

Salary

Market competitive compensation; Performance-based annual bonus scheme; Company shares welcome grant

Skills & Requirements

Must-have

  • Fluent in English listening and writing
  • 2 years clinical or drug development experience
  • BS in relevant scientific discipline preferred
  • Efficient in Microsoft Word Excel Outlook
  • Excellent organizational and prioritization skills

Nice-to-have

  • Collaborative and supportive team environment
  • Passionate interest in fighting cancer
  • Experience with CTMS and eTMF systems
  • Knowledge of Japan specific regulations
  • Ability to work independently with guidance

Key Requirements

  • Bachelor's degree in scientific discipline
  • Minimum 2 years in biotech/pharma/CRO industry
  • Fluency in English required

Work Rights

Not specified

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