ph3Company Description /h3pMedicine moves forward here.
So will you.
/pp At Prime Vigilance, patient safety is not one part of the job.
It is why we exist.
/pp 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.
/pp That work takes curious minds, problem-solvers and experts who care about getting it right.
It also takes a culture worth staying for.
Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from.
/pp If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here.
We would love to hear from you.
/ph3Job Description /h3ulli Providing support to other activities undertaken by the project team on behalf of the client and the company /lili Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency) /lili Proposes process changes to ICSR Operational Lead /lili Manages ICSR deviations with ICSR Operational Lead support /lili Reviews trackers and timesheet data and ensures accuracy /liliICSR processing and 2nd QC of cases /lili Support other departments /lili Operates as the assigned team SME /lili 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 /li /ulh3Qualifications /h3ulli Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance /lili3-4 years of work experience in pharmacovigilance within which minimum 1 year of work experience in line manager role.
/lili Excellent communication (written and verbal) skills /lili Organization skills, including attention to details and multitasking /lili Delegation skills /lili Planning and time management /lili Technical skills /lili Team working /lili English - fluent (spoken, written) /li /ulh3Additional Information /h3pWhen you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world.
You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
/pp We are diverse in many ways, yet our values unite us.
Our values are how we work, not words on a wall.
If they sound like you, you will feel at home here.
/pulli Quality: we hold ourselves to the standard patients deserve.
/lili Integrity and trust: we do the right thing, especially when it is hard.
/lili Drive and passion: we care about the outcome, because someone is waiting on it.
/lili Agility and responsiveness: we move quickly, because patients cannot wait.
/lili Belonging: everyone is welcome, and every voice counts.
/lili Collaborative partnerships: we go further by going together.
/li /ulp We look forward to welcoming your application.
/ppremote /p /p #J-*****-Ljbffr

📌 Pv Officer (Experience In Medical Devices Required) (Italia)
🏢 PrimeVigilance
📍 Italia