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Remote Clinical Trial ICSR & Pharmacovigilance Consultant

Hydrogen Group

Hydrogen Group is seeking a Clinical Trial Consultant / Pharmacovigilance Specialist for a remote EST-preferred role. The 12-month contract involves end-to-end ICSR processing, quality control, and ensuring regulatory-compliant safety reporting.

You will collaborate with Data Management and internal safety stakeholders, covering weekends as needed. The role requires a bachelor’s in science or healthcare and at least 4 years in pharmacovigilance, with experience in ArisG, Argus, or Veeva.

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Vacancy posted 4 hours ago
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