Lead clinical trial execution for a life sciences organization in Raleigh, working hybrid, with responsibility across multiple concurrent studies. Apply expertise in clinical operations and trial delivery from site activation through database lock.
This director-level clinical operations leader oversees Phase I-III studies across their full lifecycle. The work includes CRO and vendor oversight, clinical trial budgets, patient recruitment, and risk-based monitoring. You will ensure compliance with GCP, ICH guidelines, and applicable regulatory requirements while supporting portfolio delivery.

Key Responsibilities

Own trial delivery from site activation through database lockOversee Phase I-III clinical trial management activitiesManage CRO scope, budgets, performance,



and timelinesDrive recruitment, enrollment strategies, and site activationLead risk-based monitoring and quality oversightRequirements:
Director-level clinical operations leadership experienceExperience overseeing concurrent clinical studiesKnowledge of GCP, ICH, and regulatory requirementsExperience managing clinical trial budgets and forecastsExperience with clinical trial execution processesDirect clinical operations, CRO oversight, recruitment, and quality execution across Raleigh-based hybrid clinical trial programs.

📌 Director Clinical Trial Operations (Canada)
🏢 Scovai
📍 Canada