Senior Clinical Project Manager
Core
Managing cross-functional project teams to deliver high-quality ophthalmic clinical trials on budget and timeline for sponsors.
Role type
Senior Clinical Project Manager (Ophthalmic Drug/Device Development)
Builds
Clinical trial programs for ophthalmic drug and device sponsors
Domain
Ophthalmic clinical research and drug/device development
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
Clinical project management, cross-functional team leadership, protocol and source document review, project planning and timeline management, vendor management, regulatory compliance (GCP), budget and progress reporting, risk identification and mitigation, eTMF management
Preferred skills
Ophthalmology domain expertise, multi-center trial experience, Veeva TMF and CTMS systems proficiency, multi-lingual communication
Technologies
Veeva TMF, CTMS, Excel, PowerPoint
Responsibilities
Manage departmental staff including Clinical Project Managers and Clinical Trial Associates; coordinate interdepartmental groups (stats, data management, safety, regulatory, vendors); create and maintain project plans and timelines; review study metrics and prepare financial/project reports; manage vendor relationships; ensure eTMF completeness; participate in bid defenses and process improvement initiatives.
Seniority
Senior, hands-on IC with mentorship responsibilities
