Senior Pharmacovigilance Project Manager- Europe
- Role
- Project Management
- Experience
- Senior
- Employment
- Full-time
Open to PL only. Set where you work from to check your eligibility.
No BS summary
Senior pharmacovigilance project manager in Europe with hands-on PV experience, including ICSRs, aggregate reports, literature screening, reconciliation and SOPs. Needs PV project management experience, ideally from a service provider/CRO, plus healthcare professional or life science graduate background.
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.
- Acting as the primary contact point for project-related matters
- Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations.
- Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance.
- Project activities planning, including deadlines and interim milestones
- Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.
- Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
- PV Project Management experience from ideally a service provide / CRO
- Health Care Professional or Life Science Graduate
- Be comfortable with communicating at senior levels within pharmaceutical organizations
- Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving.
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.
- Quality: we hold ourselves to the standard patients deserve.
- Integrity and trust: we do the right thing, especially when it is hard.
- Drive and passion: we care about the outcome, because someone is waiting on it.
- Agility and responsiveness: we move quickly, because patients cannot wait.
- Belonging: everyone is welcome, and every voice counts.
- Collaborative partnerships: we go further by going together.
We look forward to welcoming your application.
What you'll do
- Acting as the primary contact point for project-related matters
- Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations.
- Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance.
- Project activities planning, including deadlines and interim milestones
- Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.
What they require
- Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
- PV Project Management experience from ideally a service provide / CRO
- Health Care Professional or Life Science Graduate
- Be comfortable with communicating at senior levels within pharmaceutical organizations
- Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving.
Benefits
- You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
- Quality: we hold ourselves to the standard patients deserve.
- Integrity and trust: we do the right thing, especially when it is hard.
- Drive and passion: we care about the outcome, because someone is waiting on it.
- Agility and responsiveness: we move quickly, because patients cannot wait.
- Belonging: everyone is welcome, and every voice counts.
- Collaborative partnerships: we go further by going together.
PrimeVigilance is a global pharmacovigilance specialist helping clients navigate complex regulations and patient safety from early development through post-marketing surveillance.
What people say about this company
2.5/ 5