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
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
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
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 Project Manager (Remote) Position Summary The Pharmacovigilance Project Manager / Project Lead is a senior client-facing professional responsible for the end-to-end operational management of one or more assigned pharmacovigilance client accounts at Med Communications. The
Pharmacovigilance Medical Writing Manager Position Summary The Pharmacovigilance Medical Writing Manager is responsible for writing and editing a variety of scientific and medical content, including but not limited to the following: Aggregate Reports, Risk Management
To strengthen our Commercial Sales team in Italy, we are currently hiring a Hospital Specialist (m/f/x) – Region: Puglia, Molise, Province of Potenza in Basilicata region (Fulltime / permanent) Reporting Relationships: Role that this position reports
Career CategoryMedical Affairs Job Description HOW MIGHT YOU DEFY IMAGINATION? Do more with the knowledge you’re working hard to acquire and the passion you already have. At Amgen our shared mission—to serve patients—drives all that we
Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
A leading pharmaceutical company seeks a CRM/Vault Manager to oversee the Veeva ecosystem. This autonomous role requires strategic insight and technical expertise. Responsibilities include managing system integrity and performance, addressing complex issues, and ensuring compliance. Ideal candidates should
A leading pharmaceutical company seeks a CRM/Vault Manager to oversee the Veeva ecosystem. This autonomous role requires strategic insight and technical expertise. Responsibilities include managing system integrity and performance, addressing complex issues, and ensuring compliance. Ideal candidates should
Recordati is seeking a Safety Database Associate in Milano, Italy, to support the maintenance and implementation of systems and tools for managing Pharmacovigilance activities. The role involves configuring databases, ensuring compliance, and providing user support. The ideal
Experteer Italy is looking for a member to support the Pharmacovigilance (PV) team by maintaining and implementing PV systems and tools such as Oracle Argus and Veeva Vault. Your primary duties will include configuring databases to meet new
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dellindustria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione di Laboratory Excellence è sempre in una fase di grande crescita
At Cooper Consumer Health, we’re building a legacy. Are you ready to be part of it? Cooper Consumer Health is one of Europe’s leading consumer healthcare groups, delivering trusted OTC solutions that empower healthier living every
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice
Are you a talented Clinical Trial Assistant with a passion for clinical research? Were looking for an experienced Freelance CTA to join a dynamic team supporting cutting-edge studies Key Responsibilities: Assist in the management and oversight
A leading clinical research company is seeking an experienced Freelance Clinical Trial Assistant to join a dynamic team in Milan. The ideal candidate will have at least 5 years of experience supporting global clinical project teams,
Job Purpose We are looking for a Safety Database Associate to support the team in the maintenance and implementation of all the systems and tools used for the management of the Pharmacovigilance activities. Key Responsibilities Databases/tools configuration
Pharmacovigilance Medical Writing Manager Position Summary The Pharmacovigilance Medical Writing Manager is responsible for writing and editing a variety of scientific and medical content, including but not limited to the following: Aggregate Reports, Risk Management Plan(RMP), Risk