Fortrea社招岗位

Job Overview: Prepares and negotiates and assists in the execution and retention of site agreements, confidentiality agreements, letters of indemnification and

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Summary of Responsibilities: Duties include diverse coordination and administrative tasks and activities. May organize multiple processes, procedures, or progr

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Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

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Job Overview: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Pro

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Role Summary This is a highly specialized professional focused on Taiwan post marketing PV and serving as the primary liaison with local regulatory authorities

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Job Overview: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Pro

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Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

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Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

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Fortrea is currently recruiting for an FSP Lead Data Manager for a global pharmaceutical project. This position can be based in either Beijing or Shanghai. Key

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Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, appl

学历以官网为准 · 查看完整岗位与申请入口 →