Job Description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

  • Writes, edits, and reviews documents, including informed consent forms, patient information, and other project-specific clinical documentation.
  • Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives.
  • Collects and tracks documents for CSR appendices, in support of the Quality Control Associates.
  • Performs quality control (QC) reviews of PSI-developed documents, in support of the Quality Control Associates.
  • Acts as a backup contact for the Project Managers and other PSI f...

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