Global Study Manager (Quebec City)
Insight Global
Must-Haves:
- 3+ years of clinical trial experience in pharma/life sciences
- Oncology clinical trial experience
- Experience owning or supporting end-to-end study execution (start-up to closeout)
- Robust experience managing timelines, budgets, and deliverables
- Experience leading meetings, tracking progress, and coordinating global teams
- Hands-on experience with TMF / CTMS systems
- Strong knowledge of ICH-GCP + clinical drug development lifecycle
- Experience working with CROs and external vendors (strategic level)
- Mentorship / leadership experience
- Bachelor’s degree (life sciences or related)
Day-to-Day:
- Lead or support full lifecycle of global clinical trials
- Ideally works for or has worked for a globally-located company
- Manage timelines, budgets, and study deliverables
- Partner cross-functionally (DM, Regulatory, Safety, Vendors)
- Track enrollment, data delivery, and trial progress
- Identify and mitigate risks or delays
- Oversee vendor performance and scope
- Maintain TMF quality and ensure inspection readiness
- Support IP supply and logistics
- Provide updates to leadership and stakeholders
- Drive process improvements and best practices across studies
Vacancy posted 4 hours ago
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