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Trial Operations Expert

1 tydzień temu


Warszawa, Mazovia, Polska IQVIA LLC Pełny etat
Job Summary
This position involves working as a senior-level safety scientist on various clinical trials, ensuring that all aspects of trial operations meet the highest standards. The ideal candidate will have extensive knowledge of clinical trials, data review tools, and regulatory guidelines, as well as excellent analytical and communication skills. This role requires strong leadership abilities, with the ability to lead teams and make informed decisions quickly.

Responsibilities
The primary responsibilities of this position include:
  1. Ensuring consistent processes and efficient review of critical clinical/safety data.
  2. Reviewing patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency, and generating applicable queries as needed for appropriate medical assessment and case closure.
  3. Preparing aggregated data visualization and facilitating meetings related to the review of safety data on a study level.
  4. Contributing to study start-up activities according to the applicable processes/procedures (e.g., input to applicable documents, tools setup).