Program Manager II, Clinical Research Operations, Platforms and Devices

Manage day-to-day ophthalmic Rx program and device logistics and Collaborate with cross-functional partners including Clinical, Research Scientists, UX Researchers, Hardware/Software Engineering, and Regulatory to track program and study requirements, maintain schedules, and monitor study-readiness and compliance criteria. Manage study workflows by coordinating human subject test execution, managing evaluation logistics, and supervising clinical participant and laboratory logistics alongside research scientists and program stakeholders.

Identify risks, blockers, and changing timelines early (such as recruitment bottlenecks, site enrollment delays, or regulatory hurdles), working alongside Program and Clinical Leads to triage operational issues. Contribute to team operational excellence by supporting clear clinical program tracking mechanism. Manage administrative and operational program overhead, including compiling resource demands, drafting program-related status reports.