Pharmacovigilance Support - Milan

We are seeking a Pharmacovigilance Support to join our team. As a Pharmacovigilance Support, you will be responsible for managing inbound information according to local procedures and management of ICSRs (medicinal products, food supplement, cosmetic and medical device). You will ...

As a scientific expert and pharmacovigilance resource to external and internal partners within the region, · Serve as scientific expert and pharmacovigilance resource to external and internal partners within the region. · Supports regional leads in day‑to‑day operations. · ...

The primary objective of this function is to assure the development, implementation, and maintenance of Recordati's Quality Management System in relation to Pharmacovigilance. · ...

We are searching for a brilliant Medical Information Specialist & PV Monitor with a strong scientific background and a previous experience (at least two years) in a similar role to join our Medical Affairs Department. · The new colleague will be responsible for providing accurate ...

+We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. · ...

J&J Innovative Medicine is recruiting for a Associate Director, Pharmacovigilance Audit Programme Lead. · The candidate will join the R&D Quality J&J Innovative Medicine organization focusing on RDQ QA PV audit strategies for Local Operating Companies (LOCs) and External Supplier ...

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. · Support the Head of Regional PV and EU/UK QP ...

We are searching for a brilliant Medical Information Specialist & PV Monitor to join our Medical Affairs Department. · ...

We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. · ...

The Associate Director of Quality Assurance ensures continuous quality improvement through effective management and oversight of audits and inspections. Identifies and implements IT solutions and process efficiencies. Facilitates ongoing quality improvement measures through commu ...

Medical Monitor (MD) · Location: Milan, Italy · Work Model: Full-time, On-site (5 days per week) · Position Summary · We are seeking a highly qualified Medical Monitor (MD) to join our clinical development team based in Milan. This is a full-time, on-site role requiring daily pre ...

The RQS Manager leads the Regulatory Affairs strategy and Quality Management System in Italy, · Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. · Develops and executes long- and short-term regulato ...

Responsibilities: · Support senior leadership with analysis of business performance and strategic initiatives · Assist with budgeting, forecasting, and financial reporting processes · Prepare presentations, reports, and business models for internal stakeholders · Evaluate busines ...

We are seeking a Patient Safety Monitor who will be part of the Pharmacovigilance (PV) team for the Italian territory. · Collect, review, report and follow-up on ICSRs and other safety information for all products · Maintain and review local PSMF sections or annexes as applicable ...

The Regulatory Affairs Manager is responsible for managing regulatory activities for an assigned product portfolio. · ...

+Job summary · We are seeking a Clinical Trial Associate to provide essential operational and administrative support within the Clinical team on global level.++Maintain and update SOP lists · Assign track document training activities · ...

Regulatory Affairs professional with years of experience in pharmaceutical industry supporting global clinical development programs across EU US and RoW. · ...

The RQS Manager leads the Regulatory Affairs strategy and Quality Management System in Italy. · The role involves guiding and supporting the regulatory, quality, and pharmacovigilance teams.Develops and executes long- and short-term regulatory plans in line with company objectiv ...

The Pharmacovigilance Analyst role at Viatris involves assisting with the review of PV SOPs and other department's SOPs for alignment, as well as directly involved in continuous improvement work regarding local PV procedures and tools. · ...

We help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women's health, gastroenterology, and urology.The RQS Manager leads the Regulatory Affai ...