ph3Job Title: Pharmacovigilance Support Specialist – PV Italy /h3 h3Overview: /h3 pJoin a dynamic team supporting critical pharmacovigilance activities for a prominent Italian client. As a PV Italy Support Specialist, you will play a key role in evaluating medical reports related to drugs and medical devices, ensuring patient safety and regulatory compliance across the EU. This role offers an exciting opportunity to contribute to healthcare safety initiatives while working within a collaborative environment that values expertise and precision. If you are passionate about pharmacovigilance and eager to make a meaningful impact, this position is your gateway to a rewarding career. /p h3Required Skills: /h3 ul liStrong understanding of pharmacovigilance processes, including signal detection, PSUR, RMP, and medical assessment of incidents. /li liExperience in evaluating reports linked to drugs and medical devices, with the ability to assess severity, causality, and impact. /li liKnowledge of MedDRA coding and familiarity with RCP guidelines. /li liExcellent analytical and communication skills to compile and report detailed safety evaluations.
/li liAbility to review signal detection reports and contribute to safety database management. /li /ul h3Nice to Have Skills: /h3 ul liPrior experience supporting EU or global pharmacovigilance teams. /li liExperience with notifications, follow-up requests, and safety reporting procedures. /li liFluency in Italian and English languages for seamless communication with local and international teams. /li /ul h3Preferred Education and Experience: /h3 ul liBachelor's degree in Pharmacy, Medicine, Life Sciences, or a related field. /li liPrevious experience in pharmacovigilance, medical assessment, or drug safety roles preferred. /li liIdeally, 2+ years working in a pharmaceutical or healthcare setting with regulatory compliance focus. /li /ul h3Other Requirements: /h3 ul liSome collaboration with client data management and QA teams, with potential for on-demand support. /li liThis position may require occasional communication with regulatory bodies and internal stakeholders. /li /ul /p #J-*****-Ljbffr
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