Pharma Project Specialist

il y a 2 semaines

Paris, France Healthcare & Technology International (HTI) Temps plein

Prise de poste non définie Autre Paris

Nombre de poste : 1 CDI De 50k à 60k euros

**Description du poste et des missions**:
Notre Client est une société Française innovante qui conçoit, fabrique et commercialise des équipements de diagnostic pour évaluer la santé du foie, identifier les pathologies et gérer précisément et efficacement les traitements. Non invasif (alternative à la biopsie), il permet de faire des évaluations par la résonnance d’ultrasons.

Dans le cadre de son développement, il recrute un(e):
**Pharma Project Specialist** H/F**

Poste basé au siège à Paris

Vos principales missions seront de:
**Management des clients Pharma & CROs**:

- En collaboration avec l’ensemble de l’équipe Pharma, être le point de contact des clients Pharmas et CROs de l’entreprise tout au long de leurs études cliniques
- Mettre en place la planification de ces projets (calendriers, étapes, ressources, budget )
- Organiser et mener les revues de projet avec nos clients Pharmas et CROs
- Suivre et communiquer la progression des projets (préparation, déploiement, formation )
- Gérer les interactions entre les clients Pharmas/CROs et les parties prenantes internes à l’entreprise (administration des ventes, logistique, formation, service )
- Préparer et maintenir la documentation des projets

**Support des études cliniques de nos clients Pharma & CROs**:

- Mener le processus d’initiation des études cliniques (Start Up process), incluant l’étude de qualification et de sélection des sites cliniques, la mise en place des outils de suivi, l’organisation du kick-off et des revues de projets.
- Coordonner et suivre le déploiement, la formation, le service des appareils et autres services, avec le support des différents départements (administration des ventes, logistique, formation, service ) et des partenaires et distributeurs de l’entreprise

**Mise en place de l’organisation, des outils et process**:

- Gérer les interactions avec les sites cliniques à toutes les étapes des projets, de la qualification des sites à leur fermeture, en passant par leur activation, le déploiement d’équipements, la formation et l’organisation des services cliniques
- Documenter la gestion des sites sur l’outil et mettre en place les outils de suivi et de monitoring

**Profil souhaité**:
Votre profil:

- Au minimum 3 à 5 ans d’expérience dans des groupes pharmaceutiques ou CROs et dans la gestion d’études cliniques
- Rigueur, précision exigence
- Capacité à interagir avec une multitude d’interlocuteurs avec tact mais assertivité et volonté
- Expérience en gestion d’études cliniques en CRO ou groupe Pharma
- Anglais courant impératif

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