Medicine moves forward here. So will you.
At PrimeVigilance, patient safety is not one part of the job. It is why we exist.
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-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.
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.
Role and Responsibilities
Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
Extensive experience in pharmacovigilance within which demonstrated work experience in line manager role.
When 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.
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.
We look forward to welcoming your application.
Leads ICSR case-processing teams, manages staff and project KPIs, supports case processing and quality control, and improves pharmacovigilance procedures and operational efficiency.
Leads pharmacovigilance case-processing teams, managing staff and project KPIs while overseeing ICSR processing, quality checks, deviations, and process improvements to support client projects and patient safety.
Leads the pharmacovigilance safety function and team, overseeing product risk management, safety data review, regulatory documentation and inspections, and safety governance across clinical and regulatory activities.
Leads prospective utilization review by resolving complex clinical questions, reviewing cases, auditing and coaching nurses, and managing daily case inventory, turnaround times, and team workflow.
Lead and develop the Medical Office Assistant team, overseeing staffing, service quality, performance, and workflow improvements while using operational data to support launches and enhance patient and provider experiences.
