International Pharmacovigilance Project Manager

JR France; Paris; Sur place; EUR 50 000 - 75 000; Plein temps

Résumé du poste

Une entreprise de santé en pleine croissance, Excelya, recherche un Manager de Projet en Pharmacovigilance pour rejoindre son équipe dynamique à Paris. Ce rôle implique la coordination de l'ensemble des activités de pharmacovigilance au niveau international, en veillant à ce que les systèmes des filiales respectent les exigences réglementaires locales et mondiales. Les candidats idéaux auront un diplôme en pharmacie ou en sciences de la vie, ainsi qu'une solide compréhension des exigences réglementaires PV. Si vous êtes prêt à relever des défis audacieux et à contribuer à l'innovation dans la recherche clinique, ce poste est fait pour vous.

Qualifications

• Capacité prouvée à prospérer dans des environnements collaboratifs et dynamiques.
• Connaissance solide des exigences réglementaires PV, surtout dans le contexte de l'UE/EEE.

Responsabilités

• Coordonner le réseau des responsables PV locaux dans les filiales internationales.
• Montrer et rapporter les activités clés de PV à travers les régions.
• Organiser des réunions et des formations régulières avec les équipes locales de PV.

Connaissances

Connaissance des exigences réglementaires PV

Travail en réseau international

Formation

Diplôme en pharmacie, sciences de la vie ou équivalent

Description du poste

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International Pharmacovigilance Project Manager, paris

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Client:

Excelya

Location:

paris, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

853913452198179635232761

Job Views:

2

Posted:

28.06.2025

Expiry Date:

12.08.2025

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Job Description:

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique—

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience . Our one-stop provider service model —offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Safety. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

• Coordinate the network of local PV officers across international affiliates.
• Ensure affiliate PV systems comply with local and global requirements.
• Monitor and report key PV activities across regions.
• Organize and facilitate regular meetings/training with local PV teams.
• Support affiliates maintaining a local PSMF .
• Conduct regulatory intelligence and impact analysis of new PV requirements.
• Support the EEA QPPV Office with operational tasks.
• Draft and track Safety Data Exchange Agreements (SDEAs) with commercial partners.
• Oversee service providers handling PV agreements (PVAs).
• Collaborate cross-functionally and support ad hoc PV projects as needed.

About You

At Excelya, taking audacious steps is encouraged , so we’re looking for individuals who are ready to grow with us and share our values.

• Experience: Proven ability to thrive in collaborative, fast-moving environments (talent matters most to us, minimum years not required)
• Skills: Strong knowledge of PV regulatory requirements, particularly in the EU/EEA context. Experience working with international PV networks or within a Global Safety structure is a strong asset. Experience in drafting or reviewing SDEAs and interacting with vendors is a plus.
• Education: Degree in Pharmacy, Life Sciences, or equivalent.