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Project Director

Temporary

1pertinent

Description de l'entreprise

Notre client est une organisation de recherche contractuelle (CRO) spécialisée en dermatologie et en rhumatologie .

Depuis sa création en 2000, il s’est forgé une solide réputation grâce à la qualité de ses recherches et à des services qui dépassent les attentes de ses partenaires. Basé à Montréal, il poursuit sa croissance et son expansion en Amérique du Nord et en Europe.

 

Description du poste

Au sein d’un environnement stimulant, vous collaborerez avec des collègues passionnés et rigoureux, dans une culture valorisant la collaboration, l’innovation, la fiabilité et la réactivité.

  • Vous souhaitez mettre votre expertise au service de la croissance d’une CRO spécialisée
  • Vous êtes un(e) leader engagé(e), proche des équipes
  • Vous aimez combiner la gestion de programmes cliniques et le management hiérarchique

Vos responsabilités

  • Superviser un portefeuille ou un programme d’essais cliniques mondiaux, incluant des études multicentriques avec de forts enjeux budgétaires
  • Encadrer et soutenir les chefs de projet assignés aux études (de projets à service unique à des projets complets multi-protocoles)
  • Garantir la qualité, la conformité et le respect des échéanciers pour l’ensemble du portefeuille
  • Être l’interlocuteur(trice) principal(e) auprès des clients et maintenir un haut niveau de satisfaction
  • Assurer la gestion des budgets, contrats, et prévisions financières des projets
  • Participer au développement des propositions commerciales, présentations client et réunions de défense d’offres
  • Mettre en œuvre des stratégies d’optimisation de la performance et d’innovation opérationnelle
  • Contribuer activement au coaching et à l’accompagnement des chefs de projet
  • Possibilité de prendre en charge des responsabilités de gestion hiérarchique (line management)

Qualifications

  • Minimum de 15 ans dans l’industrie, dont au moins 5 ans en CRO
  • Minimum de 10 ans en gestion de projets cliniques (de la mise en place à la clôture, incluant la gestion des fournisseurs et des services fonctionnels)
  • Expérience confirmée dans des essais de phase III multicentriques et multinationaux
  • Expérience en gestion budgétaire, suivi financier, et reporting
  • Solide expérience en supervision de projets, développement des affaires, et mentorat
  • Expérience en gestion hiérarchique souhaitée
  • Expérience en dermatologie ou en rhumatologie

Formation :

  • Baccalauréat en sciences dans un domaine pertinent
  • Maîtrise : atout
  • Certification PMP ou PRINCE2 : atout

Compétences :

  • Excellente connaissance des BPC (ICH-GCP), des exigences réglementaires de Santé Canada et de la FDA
  • Leadership, autonomie, sens stratégique et excellentes capacités de communication
  • Maîtrise de l’anglais (à l’écrit comme à l’oral) ; le français est un atout

Informations complémentaires

  • Horaire de travail flexible
  • Poste permanent à temps plein
  • Régime complet d’avantages sociaux (assurance médicale, dentaire, vision, REER, vacances, congés personnels, clinique médicale virtuelle, remboursement du transport en commun, activités sociales)
  • Possibilités continues d’apprentissage et de développement

 

Vacancy posted 18 hours ago
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