About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Pharmacovigilance Signal Detection Lead Summary The Pharmacovigilance Signal Detection Lead is a senior expert responsible for leading and executing signal detection and evaluation activities across assigned client portfolios. The role combines scientific and epidemiological expertise
Pharmacovigilance Aggregate Reporting Lead Position Summary The Pharmacovigilance Aggregate Reporting Lead is a senior expert responsible for leading, coordinating, and overseeing the preparation and submission of aggregate safety reports across assigned client portfolios. The role encompasses
Supporting Patient Safety and Pharmacovigilance Excellence At Shionogi, we are committed to improving global health through innovation, collaboration and scientific excellence. As our European organisation continues to grow, we are strengthening our pharmacovigilance capabilities to ensure
Zentiva is a pharmaceutical company specializing in the production of high-quality, affordable medicines. With a global team of more than 4,800 employees and a network of manufacturing sites in Prague, Bucharest, and Ankleshwar, we are committed
Experteer Italy, located in Rome, seeks a QA GVP Consultant to lead audits and ensure compliance with GVP regulations. Youll collaborate with cross-functional teams and assist clients in developing annual audit plans, while also overseeing day-to-day deliverables.The ideal
Overview Advarra Consulting seeks independent GxP auditors with experience in clinical research, quality assurance, and related life sciences to perform independent audits across GxP domains (GCP, GCLP, GLP, GMP, GVP, CSV). Responsibilities Auditor Engagements (may include any
Fondazione Telethon ETS (FT) is committed to developing therapeutic options for patients affected by rare genetic disorders. FT pipeline consists in various programs at different development stages (from pre-clinical to commercial). For such programs, Telethon is
Fondazione Telethon in Turbigo is looking for a Quality Assurance Associate to ensure compliance with GCP and GVP guidelines. The successful candidate will be responsible for overseeing clinical trial activities and managing quality records. The role requires
Pharmacovigilance Signal Detection Lead Summary The Pharmacovigilance Signal Detection Lead is a senior expert responsible for leading and executing signal detection and evaluation activities across assigned client portfolios. The role combines scientific and epidemiological expertise with
Pharmacovigilance Aggregate Reporting Lead Position Summary The Pharmacovigilance Aggregate Reporting Lead is a senior expert responsible for leading, coordinating, and overseeing the preparation and submission of aggregate safety reports across assigned client portfolios. The role encompasses
Experteer OverviewIn this role you will lead QA GVP audits for clients, ensuring alignment with GVP legislation and regulatory standards. You will work with cross‑functional teams to design workflows, oversee day‑to‑day delivery, and support audit readiness. The position
Per un’importante azienda farmaceutica, attiva nello sviluppo e commercializzazione di farmaci etici, siamo alla ricerca di un/una Pharmacovigilance Manager per guidare le attività di sicurezza dei prodotti e garantire la conformità normativa nazionale e internazionale. Il
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Senior PV Auditor con esperienza in farmacovigilanza e laurea magistrale scientifica. Il ruolo prevede la gestione di audit
Clinical & PV Auditor Recordati, a global pharmaceutical company founded in the 1920s, is seeking a Clinical & Pharmacovigilance Auditor to strengthen its Quality Assurance function. The role ensures compliance of clinical development activities and the
Cosmo è un’azienda innovativa focalizzata in tecnologie mediche (MedTech) attiva nello sviluppo di soluzioni basate su intelligenza artificiale, dermatologia, malattie gastrointestinali e CDMO. Collaboriamo con partner globali per migliorare la qualità delle cure e la vita
Experteer Overview In this role you will lead end-to-end execution of clinical innovation and real‑world evidence (RWE) projects within Global Clinical Development. You will collaborate with cross-functional teams to translate strategies into practical plans, ensuring quality,
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Italy, IT Responsibilities End to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Experteer OverviewAs Pharmacovigilance Consultant, you will support global PV activities to ensure regulatory compliance and patient safety. You will contribute to benefit–risk evaluation, signal management, and RMPs, and assist in PSURs/PBRERs and safety reporting. You will
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