Local QPPV_Spain

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Candidates with 3 years of Pharmacovigilance / Safety experience are welcome to apply.

Responsible for establishing and implementing the pharmacovigilance system for marketing authorization holder (MAH)/sponsor.

Maintaining and improving compliance.

Review and submit pharmacovigilance-related documents, including but not limited to PSUR/PBRER/DSUR.

Ensure the necessary quality, including the correctness and completeness, of pharmacovigilance data submitted to authorities.

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