Senior Scientific Writer - Clinical Protocols & Regulatory
Listed on 2026-10-03
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Research/Development
Clinical Research, Research Scientist, Medical Science
WELL Health Technologies Corp in Canada is seeking a Scientific Medical Writer 1 for a full-time, remote role (GTA). You will write Phase 1-4 study protocols, bioequivalence studies, and informed consent forms, and perform literature searches and regulatory discussions.
You will collaborate with PK scientists, biostatisticians, and regulatory agencies to ensure GCP compliance and timely study design. A PhD and 3+ years of protocol writing, plus CRO experience, are required, with excellent
This opening is for the Senior Scientific Writer
- Clinical Protocols & Regulatory role at WELL Health Technologies Corp.
As a Senior Scientific Writer
- Clinical Protocols & Regulatory, you will play an important part at WELL Health Technologies Corp in Toronto, ON, Canada.
We invite applications for the Senior Scientific Writer
- Clinical Protocols & Regulatory position located in Toronto, ON, Canada.
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