Job Description

The Clinical Trial Associate I (CTA) is an essential part of the Local Study Team and is responsible for supporting key site and country level clinical trial tasks for assigned studies to ensure compliance with timelines, GCP, Pfizer SOPs and country regulations. The role collaborates with local study team members and is responsible for multiple tasks that span from study start-up to study close-out inclusive of site invoice support which enables the efficient execution of clinical trials to high quality standards.

The CTA I:

  • Works independently to carry out key tasks using established procedures and methodologies to ensure the completion according to timelines and to required quality standards.
  • Contributes to best practices within the team to ensure efficient task support with a high quality output.
  • Can deliver specialist work.

    • ROLE RESPONSIBILITIES

    With direction, the CTA I is responsible for providing technical and operational supp...

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