Senior Pharmacovigilance Project Manager- Europe

PrimeVigilance; Guildford; On-site; GBP 45,000 - 65,000; Full time

Job summary

PrimeVigilance in Guildford is seeking a Pharmacovigilance Project Manager to lead client-facing PV projects. You will manage project scope, timelines, and deliverables, ensuring the services meet or exceed client expectations.

Your role includes coordinating cross-functional teams and preparing regular progress reports for clients. Ideal candidates will have PV management experience in a service provider setting, strong leadership, and excellent communication with senior stakeholders in the

Qualifications

• Proven track record of pharmacovigilance activities including processing and quality review of ICSS, writing or contributing to aggregate reports, literature screening, reconciliation, and SOPs.
• PV project management experience from a service provider or CRO.
• Health care professional or life science graduate with strong communication skills.
• Comfortable communicating at senior levels within pharmaceutical organizations.
• Leadership capabilities including planning, mentoring, meeting facilitation, communication and problem solving.

Responsibilities

• Acting as the primary contact point for project-related matters
• Managing client’s expectations to ensure satisfaction with PrimeVigilance services
• Preparing project scope and objectives based on the signed agreement
• Project activities planning, including deadlines and interim milestones
• Reporting for the client and PrimeVigilance management, including monthly reports and invoicing basis

Skills

Pharmacovigilance

Communication

Leadership

Project planning

Stakeholder management

Education

Healthcare professional or life science graduate

Job description

Company Description Medicine moves forward here. So will you.

Company Description 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.

Job Description

• 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.

Qualifications

• Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSS, 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.

Additional Information 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.