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Qualified Person for Pharmacovigilance
OCUGEN OPCO INC
Amsterdam · On-siteSenior (5–10 years)OtherPosted 8 days ago
About the job
What you'll do
The QPPV will establish and maintain a compliant European pharmacovigilance system in accordance with EMA Good Pharmacovigilance Practices. They will provide safety expertise for clinical development programs and manage regulatory submissions, vendor oversight, and cross-functional collaboration.
What they're looking for
Candidates must hold an advanced degree in a scientific discipline and possess 7–10 years of progressive experience in pharmacovigilance within the biotechnology or pharmaceutical industry. Expertise in EMA regulatory environments and experience supporting clinical development and regulatory inspections are required.
Full description