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Patient safety manager

Pavia
Randstad Italia
Pubblicato il 1 novembre
Descrizione

PRandstad Office Milan is looking for a /ppbr/ppbPATIENT SAFETY MANAGER /b /ppfor our pharmaceutical partner. /ppbr/ppbContract Type /b: fixed-term contract for one (1) year. /ppbr/ppbWorking Model: /b hybrid work model with 2 days of smart working per week. /ppbr/ppbRemuneration /b: commensurate with experience gained in the pharmaceutical sector and in the Pharmacovigilance Manager role (up to 70K) + voucher meal ticket (10€). /ppRAL 50.000€ - 65.000€. /ppbr/ppbResponsability /b /ppbr/ppThis role provides crucial support to the Affiliate Head of Patient Safety (AHoPS), working closely with both local and global teams. The Manager is responsible for various aspects of pharmacovigilance (PV) coordination and execution at the affiliate level, potentially acting as the named deputy AHoPS/Local Legal PV Responsible Person, in line with local legal requirements. /ppbr/ppThe position is integral in ensuring strong engagement and integration of Patient Safety within the local business. /ppbr/pullistrategic PV Partner: brings local insights to safety decision-making, including benefit/risk assessments and risk management development; /liliprogram oversight: partners on local projects (e.g., Patient Support Programs, Market Research) to ensure compliant safety solutions; /liliregulatory compliance: acts as the local safety contact point, contributing to PV audits/inspections and ensuring local PV activities comply with standards; /liliexpert knowledge: maintains expert knowledge of local PV regulations, interpreting their impact and communicating changes to the global team; /lilisafety communication: submits or delegates submission of relevant safety information to authorities (e.g., PSUR, RMP); /liliquality training: acts as the Patient Safety ambassador, providing training, and ensuring local QMS elements (including the Pharmacovigilance System Master File) are maintained; /lililocal legal role: maintains expert local knowledge and oversight of marketed product safety profiles and local studies. /li /ulpbr/ppbRequirements /b /ppbr/pulliconfirmed practical experience in pharmacovigilance; /lilicomprehensive understanding of drug safety regulations and obligations; /liliability to work with a high degree of autonomy; /liliproven leadership or influencing skills; /liliexcellent communication skills; /lilivery good written and spoken English; /liliability to represent the company externally. /li /ulpbr/pp-- /ppbr/ppThe search is open to both male and female candidates (L.903/77). Please read the privacy policy pursuant to Article 13 of Regulation (EU) 2016/679 on data protection (GDPR) at /p

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