Spécialiste de la mise en route des sites/ Site Activation Specialist

IQVIA seeks a Site Activation Specialist to manage feasibility assessments, site identification, regulatory affairs, and site startup activities across Canada. The role involves preparing documentation, negotiating contracts, tracking performance metrics, and serving as primary liaison for investigator sites.

Responsibilities

• Serve as single point of contact for site feasibility, activation, and maintenance activities in assigned studies
• Prepare, review, and verify site documentation for completeness, accuracy, and consistency
• Review, track, and follow up on regulatory documents, contracts, ethics approvals, and informed consent forms
• Update and maintain internal systems, databases, tracking tools, and project timelines with accurate information
• Distribute completed documents to sites and internal project team members; establish project schedules

Requirements

• Bachelor's degree in life sciences or related field
• 1–3 years clinical research experience or equivalent combination of education and training
• 3 years healthcare environment experience or equivalent background
• Knowledge of regulatory requirements, SOPs, and project management
• Document management and database maintenance skills
• Ability to work with moderate supervision in bilingual context