Pharmacovigilance Specialist

2 settimane fa


Milan, Italia Altro A tempo pieno

Join our team as Pharmacovigilance Specialist (remote) and embark on a new adventure in an international, dynamic environment where you can meet your career expectations in a fast‑growing organization.Your missionsSupport end‑to‑end ICSR case processing activities for established products and rare disease portfoliosPerform data entry of adverse events in compliance with regulatory requirementsConduct case validation and ensure accuracy of collected informationPerform quality checks of ICSR data, ensuring narrative and medical coding consistencyDistribute cases to commercial partners and regulatory authorities (EMA, MHRA, FDA) in a timely mannerManage follow‑up activities for ongoing casesEnsure compliance with global safety reporting workflows and timelinesMaintain accurate and thorough documentation of all case processing activitiesYour profileExperience: 2–3 years in Pharmacovigilance with solid exposure to ICSR case processingExperience in data entry, case validation, and follow‑up managementExperience in quality checking ICSR data and ensuring narrative/medical coding consistencyExperience in distributing cases to commercial partners and, ideally, regulatory authorities (EMA, MHRA, FDA)Experience with Argus Safety Database is preferredUnderstanding of GVP Modules relevant to case processingKnowledge of global safety reporting workflows and compliance requirementsAcademic background: Life Sciences, Pharmacy, Medicine, or related fieldFluent English for global communication and safety documentation; good knowledge of Italian languageAccuracy, attention to detail, and strong documentation skillsAbility to work with minimal supervision while maintaining high‑quality deliverablesWhat we offerAn international community bringing together 110+ different nationalitiesAn environment where trust has a central place; 70% of our key leaders started their careers at the first level of responsibilitiesA robust training system with our internal Academy and 250+ available modulesA vibrant workplace that frequently gathers for internal events (after‑works, team building, etc.)Strong commitments to CSR, notably through participation in our WeCare Together programRemote policy: possibility to work fully remotelyWe’re proud to be an equal‑opportunity workplace and are committed to promoting diversity within the workforce and creating an inclusive environment. All qualified candidates are welcome.Seniority level: Mid‑Senior level.Employment type: Full‑time.Job function: Management and Manufacturing.Industries: IT Services and IT Consulting.Referrals increase your chances of interviewing at Amaris Consulting by 2×.#J-18808-Ljbffr



  • Milan, Italia Altro A tempo pieno

    A global healthcare company is seeking a Pharmacovigilance Support specialist in Milan, Italy. This role involves managing inbound information regarding medicinal products and translating reports into English. Candidates should hold a Bachelor’s Degree in Scientific Disciplines and possess knowledge in pharmacology. Proficiency in both English and Italian...


  • Milan, Italia Informatica Software A tempo pieno

    A global technology consulting firm based in Milan is seeking a Pharmacovigilance Specialist to support ICSR case processing in a dynamic environment. The ideal candidate will have 2-3 years of experience in Pharmacovigilance, including data entry, case validation, and quality checks. Fluency in English and knowledge of Italian are required. This role offers...


  • Milan, Italia Altro A tempo pieno

    A global technology consulting firm is seeking a Senior Pharmacovigilance Specialist to support case processing activities and ensure compliance with safety reporting workflows. The ideal candidate will have at least 6 years of experience in Pharmacovigilance, strong attention to detail, and familiarity with regulatory authorities such as EMA and FDA. This...


  • Milan, Italia Altro A tempo pieno

    A global technology consulting firm is seeking a Senior Pharmacovigilance Specialist to support case processing activities and ensure compliance with safety reporting workflows. The ideal candidate will have at least 6 years of experience in Pharmacovigilance, strong attention to detail, and familiarity with regulatory authorities such as EMA and FDA. This...


  • Milan, Italia Informatica Software A tempo pieno

    A global consulting firm seeks a Senior Pharmacovigilance Specialist to join their international team in Milan. In this remote role, you'll support ICSR case processing activities and ensure adherence to safety reporting standards, leveraging your experience in the field. The ideal candidate has over 6 years in Pharmacovigilance and strong documentation...


  • Milan, Italia Altro A tempo pieno

    Join our team as Pharmacovigilance Specialist (remote) and embark on a new adventure in an international, dynamic environment where you can meet your career expectations in a fast‑growing organization.Your missionsSupport end‑to‑end ICSR case processing activities for established products and rare disease portfoliosPerform data entry of adverse events...


  • Milan, Italia Altro A tempo pieno

    A leading pharmaceutical company in Milan is seeking a Pharmacovigilance Specialist to assist in reviewing SOPs, train teams, and participate in audits. The ideal candidate will have a Bachelor's Degree in a scientific discipline, at least 3 years of experience in pharmacovigilance, and fluency in English and Italian. The role offers competitive salaries and...


  • Metropolitan City of Milan, Italia Cosmo I Building Health Confidence A tempo pieno

    The Pharmacovigilance (PV) Specialist supports the Marketing Authorisation Holder (MAH) entities of the Cosmo group ensuring their compliance with pharmacovigilance duties of the MAH.The role acts as the key liaison point between Cosmo and the external, contracted pharmacovigilance (PV) service providers, managing pharmacovigilance responsibilities with...


  • Milan, Italia Altro A tempo pieno

    A global healthcare organization is seeking a Pharmacovigilance Support role in Milano, Italy. The successful candidate will manage inbound information, liaise with stakeholders, and ensure compliance. The role requires a minimum Bachelor's degree in a scientific discipline, proficiency in English and Italian, and strong analytical and decision-making...


  • Milan, Italia Cosmo I Building Health Confidence A tempo pieno

    The Pharmacovigilance (PV) Specialist supports the Marketing Authorisation Holder (MAH) entities of the Cosmo group ensuring their compliance with pharmacovigilance duties of the MAH.The role acts as the key liaison point between Cosmo and the external, contracted pharmacovigilance (PV) service providers, managing pharmacovigilance responsibilities with...