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FortreaNew
Overview
Manage end-to-end pharmacovigilance activities, including processing adverse event reports from clinical and post-marketing sources. Ensure timely regulatory reporting, maintain safety databases, and coordinate follow-up for missing information.
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Compensation
Salary not listed
Posted
New
Everest Clinical Research
The Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
CA$65,000 - CA$100,000 / YEAR
5 months ago
