Clinical Trials Project Coordinator

4 weeks ago


Foster City, California, United States ATR International Full time
Job Summary

ATR International is seeking a highly organized and detail-oriented Clinical Trials Project Coordinator to support the Biomarker and Bioanalytical Operations team. The successful candidate will be responsible for tracking and preparing study-specific information, reviewing and participating in the quality assurance of data and/or documents, and arranging meeting logistics and agendas.

Key Responsibilities:

  • Track and prepare study-specific information using databases, spreadsheets, and other tools.
  • Review and participate in the quality assurance of data or documents.
  • Arrange meeting logistics, agendas, and assist with minutes.
  • Interact with other departments, as needed, to complete assigned tasks.
  • Assist with development of documents and standard forms.
  • Ensure own work complies with established practices, policies, and processes, and any regulatory or other requirements.

Requirements:

  • MA / MS / PharmD / PhD with some relevant clinical or related experience in life sciences.
  • BA / BS / RN with 1 or more years' relevant work experience.
  • Some general clinical or business knowledge and experience is preferred.
  • Working knowledge and experience with Word, PowerPoint, and Excel.
  • Excellent verbal, written, interpersonal, and presentation skills are required.

Benefits:

  • MEC/ACP Medical.
  • Voluntary Dental, Vision, Life, Supplemental Income.
  • 401k (must meet requirements).
  • Sick leave as required by state/county.


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