IQ

Gestionnaire associ(e) de l'activation des sites/Associate Site Activation Manager

Mississauga, Peel region
On-site
Full-time
No salary posted1 weeks ago
Employment type
Full-time · On-site
Posted
September 24, 2026
NOC code
21230
Province
Ontario (ON)

Hiring confidence: Sparse posting · 11/100

This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored

Job Overview

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Mississauga, Ontario, Canada Montreal, Quebec, Canada Full time R1566989 Internal Job Description Pour être éligible à ce poste, vous devez résider dans le même pays/la même région commerciale où se trouve l'emploi Location: Canada, Télétravail Aperçu du poste Diriger et gérer la réalisation de toutes les activités requises d'activation des sites, de maintien et de conformité réglementaire pour les études sélectionnées ou les programmes multiprotocoles, y compris les activités préalables à l'…

This role is based in Ontario. The Canadian NOC code for this position is 21230. IQVIA is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.

Market context

About this role in Ontario

Average salary for Gestionnaire associ(e) de l'activation des sites/Associate Site Activation Manager in Ontario

We do not have a salary benchmark for this title in Ontario yet. The posting does not state a salary either.

NOC code

21230. The National Occupational Classification code is what Express Entry, provincial nominee programs and Job Bank use to identify this occupation.

Typical qualifications for Canadian employers

  • Residence in Canada (same country/business region as job location)
  • Eligibility to work in Canada
  • Fluency in French and English
  • Knowledge of regulatory compliance for clinical studies

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Site activation management
  • Project management
  • Regulatory compliance

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What you'll do

  • Lead and manage site activation activities for selected studies
  • Oversee pre-activation activities
  • Manage multi-protocol programs
  • Ensure regulatory compliance
  • Maintain site compliance standards
  • Coordinate between multiple stakeholders
  • Manage documentation and records for clinical trials

What you'll need

  • Residence in Canada (same country/business region as job location)
  • Eligibility to work in Canada
  • Fluency in French and English
  • Knowledge of regulatory compliance for clinical studies

About the Company

IQ

IQVIA