Project Manager, Vendor Management / Gestionnaire de projet, gestion des fournisseurs
Core
Coordinate clinical research projects and oversee vendor management throughout the study lifecycle, ensuring compliance with GCP, regulatory requirements, and project timelines.
Role type
Project Manager I (Clinical Research & Vendor Management)
Builds
Clinical studies and vendor services for pharmaceutical, biotechnology, and CRO clients
Domain
Clinical Research / Pharmaceutical / Biotechnology
Required skills
Clinical trial management, Vendor oversight, GCP/ICH standards, Regulatory compliance, Project coordination, Risk management, Budget tracking, Site activation support, Data management collaboration, Quality assurance
Preferred skills
French language proficiency, Experience with site selection and qualification, Investigator meeting planning, TMF management (via careerplan.io/jobs/15-003-88-37E-project-manager-vendor-management-gestionnaire-de-projet-gestion-des-fournisseurs)
Technologies
Microsoft Office suite, Electronic Case Report Forms (eCRF), Trial Master File (TMF)
Responsibilities
Coordinate tasks and deadlines between departments; oversee project coordinators and SSU team members; manage vendor scope, timelines, and performance; ensure compliance with SOPs and regulations; monitor patient recruitment and site status; support clinical monitoring activities; manage vendor invoices and change orders; track vendor KPIs and risks; assist with quality reviews and audits.
Seniority
Junior/Mid-level, hands-on IC