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Clinical Trial Manager I

Bristol Myers Squibb · Shanghai, China

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Clinical OperationsFull-timeCompany career page

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Role summary

Bristol Myers Squibb seeks a Clinical Trial Manager I in Shanghai to manage clinical operations and ensure compliance with regulatory guidelines. The role requires expertise in GCP, ICH Guidelines, and clinical research processes, with proficiency in trial management systems and strong organizational abilities.

What they're looking for

  • Thorough understanding of GCP, ICH Guidelines, and China regulatory environment
  • In-depth knowledge of clinical research processes, regulations, and methodology
  • Practical knowledge of medical settings and medical records management
  • Demonstrated organizational, planning, and independent decision-making skills
  • Critical thinking and risk analysis capabilities
  • Proficiency with Microsoft Suite, CTMS, eDC, and eTMF systems
  • Strong verbal and written communication in English and Mandarin Chinese

What you'll be doing

  • Manage clinical trial operations and coordinate with internal and external stakeholders
  • Ensure compliance with GCP standards and country regulatory requirements
  • Oversee clinical research processes and documentation management
  • Handle multiple competing priorities with strong organizational discipline
  • Manage medical records and maintain trial master files

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What RoleLantern checked

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Date posted5 days ago
Last source checkToday
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