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

IQVIA · Quebec, Canada

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Clinical OperationsFull-time$61k–$102kCompany career page

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Role summary

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.

What they're looking for

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

What you'll be doing

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

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Date posted4 days ago

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