Milan, Italy | Full time | Hybrid | R1552789

Join IQVIA's Lifecycle Safety team and lead a growing Pharmacovigilance function supporting pharmaceutical and biotech clients. This is an excellent opportunity for an experienced PV professional to combine people leadership, client partnership and operational oversight in a highly visible role.

What you'll do

- Lead and develop a small Pharmacovigilance team, providing coaching, mentoring and day-to-day management
- Ensure delivery of high-quality pharmacovigilance and medical information activities
- Act as a key contact for clients and internal stakeholders across multiple projects
- Support regulatory compliance and inspection readiness across PV processes
- Oversee adverse event and safety case management activities
- Contribute to quality management, process improvements and operational excellence initiatives
- Support business growth through client relationship management and proposal activities
- Deliver PV training and guidance to internal and external stakeholders

What we're looking for

- Bachelor's or Master's degree in Life Sciences or a related field
- Significant experience in Pharmacovigilance within a CRO, pharmaceutical or healthcare environment
- Previous people management experience
- Strong knowledge of European pharmacovigilance regulations and processes
- Experience managing client relationships and stakeholder engagement
- Excellent communication skills in English
- Ability to work independently, prioritize effectively and lead teams in a dynamic environment

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.



We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is 53 200,00 € - 79 800,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or tempo parziale). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

📌 Pharmacovigilance Manager (Italia)
🏢 Iqvia
📍 Italia