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.
#J-18808-Ljbffr$80k - $200k
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