Pharmacovigilance manager Work, Jobs in Guildford, Sry (with Salaries)

Senior Pharmacovigilance Project Manager- Europe
PrimeVigilance —Guildford
- Full-time
- Remote
- Leadership
Quick apply
Associate Case Processing Manager (Line Management position)
PrimeVigilance —Guildford
- Full-time
- Hybrid work
- Nursing
- Team management
- Quality control
Quick apply
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
PV Specialist
Novo Nordisk —Gatwick Airport
- Computer literacy
- English
- Computer skills
7d
Senior Clinical Trial Case Manager
CSL Behring —Maidenhead
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Associate Director, People Operations (Europe)
Ergomed —Guildford
- Full-time
- Hybrid work
- English
- Human resources
- Training & development
Quick apply
EDC Developer, Zelta v2.0 Certified (Full-time 6-month contract)
Ergomed —Guildford
- Full-time
- Remote
- Bachelor's degree
- Communication skills
Quick apply
6d
ACCQM
Fortrea —Maidenhead
- Full-time
- Bachelor's degree
- Continuous improvement
- Quality control
6d
Pharmacy Business Manager
IQVIA —Basingstoke
- Full-time
- Microsoft Powerpoint
- CRM software
- Business development
- Annual leave
- Employee discount
9d
Manager - Regulatory Affairs Lifecycle Management - Medicines
Perrigo —London
- Hybrid work
- Marketing
- English
- Continuous improvement
Equine Brand Veterinary Adviser
BI AH UK Ltd —Bracknell Forest
- Full-time
- English
- Training & development
- Communication skills

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pharmacovigilance manager jobs near guildford, sry

Senior Pharmacovigilance Project Manager- Europe

PrimeVigilance -
Guildford

Quick apply

Job details

Full-time

Qualifications

Report writing
Project planning
Project leadership
Leadership
Project management experience

Full job description

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 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.

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.

Quick apply

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pharmacovigilance manager jobs in guildford, sry

Senior Pharmacovigilance Project Manager- Europe

Associate Case Processing Manager (Line Management position)

Medical Affairs Coordinator

PV Specialist

Senior Clinical Trial Case Manager

Associate Director, People Operations (Europe)

EDC Developer, Zelta v2.0 Certified (Full-time 6-month contract)

ACCQM

Pharmacy Business Manager

Manager - Regulatory Affairs Lifecycle Management - Medicines

Equine Brand Veterinary Adviser

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