Job Description

Role Summary:

The Clinical Study Team Associate (CSTA I) is an essential part of the Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and Pfizer SOPs. The role collaborates with global study team members and is responsible for multiple tasks that span from study start-up to study close-out which enables the efficient execution of clinical trials to high-quality standards.

The Clinical Study Team Associate (CSTA I):

  • Partners with the Clinical Study Team Lead (CSTL) in providing study level operational leadership and support to clinical study teams.
  • Partners with the Global Study Manager and the Study Manager in providing site management, monitoring and vendor operational oversight and support.
  • Works proactively with minimal oversight to coordinate and prioritize multiple key study tasks in support of clinical trial systems and processes.
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