Study Manager

2 days ago

Beijing, Beijing, China Parexel Full time

Key Accountabilities
General Accountabilities

  • Build and maintain engagement with Investigators, other site staff in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out.
  • Ability to manage studies and processes to agreed quality and timelines.
  • Ability to proactively identify & mitigate risks around study/site level in study execution.
  • Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies.

Compliance with Parexel standards

  • Complies with required training curriculum
  • Completes timesheets accurately as required
  • Submits expense reports as required
  • Updates CV as required
  • Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements

Skills

  • Previous experience in scientific and/or regulatory medical writing.
  • Strong Communication Skills

Knowledge And Experience

  • Keen problem-solving skills.
  • Fluent in both oral and written English.
  • Fluent in host country language required.
  • At least 5 years in clinical practices

Education

  • Minimum of BS/BA in a biomedical discipline or equivalent education/training is required

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