Emplois actuels liés à Pharmacovigilance Officer - Paris, Île-de-France - Excelya
-
Pharmacovigilance Officer Compliance F/H
il y a 5 jours
Paris, Île-de-France SERB Temps pleinCome and Save Lives with UsSERB is a fast-growing specialty pharmaceutical company that equips healthcare providers worldwide with life-saving medicines for patients facing rare conditions and emergencies.For over 30 years we have consistently provided emergency medicines, medical countermeasures, and the world's leading portfolio of antidotes.Today SERB has...
-
Senior Safety Officer
il y a 7 jours
Paris, Île-de-France Excelya Temps pleinJoin 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 join our dynamic and ambitious Pharmacovigilance and Safety team. Rooted in a long-standing tradition of...
-
Senior Safety Officer
il y a 1 semaine
Paris, Île-de-France Excelya Temps pleinJoin 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 join our dynamic and ambitious Pharmacovigilance and Safety team. Rooted in a long-standing tradition of...
-
Chargé.e PV compliance
il y a 2 semaines
Paris, Île-de-France Calypse Temps pleinLe/la chargé.e de Pharmacovigilance Compliance assiste le service Pharmacovigilance / Matériovigilance/ Médical au quotidien et s'assure de la bonne compliance de ces activités.En tant que Chargé de Pharmacovigilance / Pharmacovigilance Officer, vos responsabilités incluront entre autres :❖ VigilancesGestion des cas de vigilance : réception des...
-
Chef de Projet Opérations Cliniques H/F
il y a 5 jours
Paris, Île-de-France MSD France Temps pleinJob DescriptionContrat de stage – merci d'indiquer sur votre CV la date et la durée de votre stage.Mission générale de la fonctionConstitution des dossiers réglementaires Essais cliniques (Demande d'Autorisation d'essais Cliniques et demande de Modifications Substantielles) pour évaluation dans le cadre du règlement (EU) No 536/2014.Suivi des...
-
Chef de Projet Opérations Cliniques H/F
il y a 5 jours
Paris, Île-de-France MSD Temps pleinJob DescriptionContrat de stage – merci d'indiquer sur votre CV la date et la durée de votre stage. Mission générale de la fonctionConstitution des dossiers réglementaires Essais cliniques (Demande d'Autorisation d'essais Cliniques et demande de Modifications Substantielles) pour évaluation dans le cadre du règlement (EU) No 536/2014.Suivi des...
-
Chef de Projet Opérations Cliniques H/F
il y a 5 jours
Paris, Île-de-France MSD Temps pleinJob DescriptionContrat de stage – merci d'indiquer sur votre CV la date et la durée de votre stage.Mission générale de la fonctionConstitution des dossiers réglementaires Essais cliniques (Demande d'Autorisation d'essais Cliniques et demande de Modifications Substantielles) pour évaluation dans le cadre du règlement (EU) No 536/2014.Suivi des...
-
Attaché à la promotion du médicament H/F
il y a 7 jours
Paris, Île-de-France REPSCO Temps pleinPrise de poste : 05/01/2026 Diplôme de visiteur médical (VM) ParisNombre de poste : 1 CDD (6 mois renouvelables) De 40k à 50k eurosDescription du poste et des missionsREPSCO recrute un/une Attaché(e) à la Promotion du Médicament pour le compte d'un laboratoire partenaire :Secteur : IDF75p / 93p / 77p / 95pPrincipales responsabilitésInformation...
-
Medical Monitor
il y a 2 jours
Paris, Île-de-France PSI CRO Temps pleinCompany Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...
-
Stage Communication
il y a 2 semaines
Paris, Île-de-France Ipsen Temps pleinTitle:Stage Communication (6 mois à partir de janvier Paris - H/FCompany:Ipsen Pharma (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S.,...
Pharmacovigilance Officer
il y a 2 semaines
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 Pharmacovigilance. 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:
- Supervise pharmacovigilance case management outsourced to assigned platform(s)
- Respond to case-related emails and inquiries from external service providers
- Monitor case processing timelines and investigate any delays in reporting or transmission
- Participate in weekly quality control of data entry, MedDRA coding, and narrative writing
- Support the review and validation of clinical study case narratives for inclusion in study reports
- Contribute to the reconciliation of PV cases with business partners per Safety Data Exchange Agreements (SDEAs)
- Oversee reconciliation of cases with clinical databases managed by outsourced providers
- Collaborate closely with cross-functional and global teams to ensure compliance and data integrity
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)
- Skills: Solid understanding of global PV regulations and quality systems, experience in managing CAPAs, deviations, and regulatory compliance indicators, familiar with the preparation and conduct of audits and inspections (internal and external).
- Education: Doctor of Pharmacy (PharmD) degree required.
- Languages: Fluent in written and spoken English and French; strong communication skills with global teams.
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.