Sr Staff Clinical Technical Program Manager, APAC
Core
Lead planning and execution of complex, multi-country clinical studies for diabetes CGM technology across the Asia Pacific region.
Role type
Sr Staff Technical Program Manager (Clinical Affairs)
Builds
Clinical study programs supporting product development and regulatory submissions for medical devices
Domain
Medical Devices / Diabetes Care / Clinical Research
Required skills
Clinical research regulations (GCP), multi-country program leadership, protocol design, CRO management, risk mitigation, budget/timeline management, stakeholder alignment
Preferred skills
Diabetes/digital health device studies, APAC market regulations, process improvement, Microsoft Project/Smartsheet
Technologies
Microsoft Excel, Word, PowerPoint, Microsoft Project, Smartsheet
Responsibilities
Lead full lifecycle of clinical studies from protocol design to closeout; Manage study operations including timelines, budgets, and KPIs; Coordinate activities across multiple studies; Identify and mitigate study risks; Drive selection and management of CROs; Develop study documentation (CIPs, ICFs, CRFs); Oversee study startup and site initiation; Develop executive reports and dashboards; Champion process improvements
Seniority
Sr Staff, hands-on IC with strategic leadership
