Senior Scientific Writer - Clinical Protocols & Regulatory (Quebec City)

03 Oct

WELL Health Technologies

Quebec City

03 Oct

WELL Health Technologies

Quebec City

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

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📌 Senior Scientific Writer - Clinical Protocols & Regulatory (Quebec City)
🏢 WELL Health Technologies
📍 Quebec City

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