Medicine moves forward here. At PrimeVigilance, patient safety is not one part of the job. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance.

Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on. That work takes curious minds, problem-solversand experts who care about getting it right.

Across

Europe, North America, South America,Asiaand Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another andgood ideasare heard wherever they come from. Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader and Line Manages ICSR staff Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management Works under supervision ofICSR Operational Lead Providing support to other activities undertaken by the project team on behalf of the client and the company Createsand maintainsproject specific KPIs for contracted ICSR activities (this includes optimizing procedures,



trainings and any other actions to increase ICSR team efficiency) Is involved inICSR processingand2nd QC of cases Support other departments, as approved and instructed by ICSR Operational Lead Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance Strong previouswork experience in pharmacovigilance within which minimum 1 year of work experience in line managerrole.

Medical

Device experience required Planning and time management English – fluent (spoken, written) Advanced literacy (MS Office) When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world.You'lljoin a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. Our values are how we work, not words on a wall. Integrity and trust:we do the right thing, especially when it is hard.

Drive and passion:we care about theoutcome, becausesomeone is waitingonit. Collaborative partnerships:we go further by going together. . #

📌 Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience need (Roma)
🏢 Ergomed
📍 Roma