Global Study Manager

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 → closeout) Strong 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