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)
• 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)
• Tr...