Jack Oreilly

Eea Qualified Person for Pharmacovigilance @ProPharma

Berlin, DE

EMAILS

[email protected]

MOBILE NUMBERS

+91 *********19

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WORK HISTORY

Feb 2021 — Present

Eea Qualified Person for Pharmacovigilance @ProPharma

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Fulfilling the role of client manager and EEA QPPV for their clients I work to ensure compliance with both Internal and Client processes as well as ensuring compliance with EU Legislation and provide full fulfilment of the EU QPPV role on a continual basis. Key achievements: • Provision of 24/7 EEA QPPV service for various clients • Oversight of PV systems for various clients • PSMF oversight • Client management support for various clients • PV process review and…

SKILLS

Regulatory RequirementsManagementChange ControlRisk ManagementEctdLifesciencesBiotechnologyRegulatory AffairsCROProject ManagementRegulatory SubmissionsGood Clinical Practice (Gcp)PharmacovigilanceOncologyTeam LeadershipStandard Operating Procedure (Sop)Quality SystemFdaMedical DevicesClinical DevelopmentCapaGmpPharmaceutical IndustryClinical TrialsTechnology TransferBiopharmaceuticalsTrainingPharmaceuticsSopTeam Mentoring

ABOUT JACK OREILLY

Pharmaceutical professional with over 14 year’s industry experience specialising in…

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