17 set - Italia
Chiesi
Overview In this role you will support GRAPS to ensure the pharmacovigilance system aligns with regulatory expectations. Based at the Parma headquarters with hybrid work, you will help maintain PSMF readiness, monitor PV KPIs, and report on global PV performance. You will interact with stakeholders worldwide to implement PV improvements and advise on changes to keep the system compliant. This is a chance to shape pharmacovigilance processes within a global, sustainability-focused organization.
Retribuzione / Benefits
pension
private medical insurance
wellbeing programme
flexible benefits programme
remote work options
annual premio scheme
Responsabilità
Evaluate and apply pharmacovigilance regulations and guidelines to the company's PV system
Ensure the PSMF is up-to-date by collecting stakeholder documents and advising on amendments
Contribute to defining and improving PV KPIs and monitoring/reporting processes
Track PV metrics and trends, address compliance issues, and support issue resolution
Deliver KPI and PSMF reports to stakeholders for Global PV system assessment
Collaborate with QPPV and other stakeholders on PV system improvements
Requisiti fondamentali
Master Degree in life sciences, pharmacy or related fields
Minimum 5 years of international Pharmacovigilance experience in pharma/biotech or CRO
Proven ability in effective communication
Strong decision making and problem solving
Team working and cross-functional collaboration
Effective communication
Decision making
Team working
Pharmacovigilance regulations and guidelines
PSMF management and governance
PV KPI definition and reporting
18 set - Chiavari
Acrobatica
18 set - Fonzaso
Greta
18 set - Trento
Car Clinic
18 set - Nola
Demetra Formazione