Clinical Project Manager I provides project management support across assigned clinical studies within one or more Voiant service lines, including Medical Imaging (IMG), Endpoint Adjudication Committees (EAC), and Ophthalmology (OPH). Operating under regular guidance from the Associate Director or Sr. CPM, the CPM I is accountable for executing study deliverables, maintaining cross-functional coordination, and developing toward increasingly independent study management. This role serves as the entry point to the Clinical Delivery career track and is expected to build foundational competency across Voiant systems, sponsor communication, and regulatory standards.
Responsibilities & Accountabilities
Manages an assigned portfolio of clinical studies under regular guidance from the Associate Director or designee, developing toward increasingly independent study execution as experience and competency grow.
Develops, maintains, and manages all study-specific documentation and deliverables applicable to assigned studies, including study execution plans,
data review plans, imaging charters, timelines, and status reports; may consult with the Associate Director or designee for guidance as needed.
Serves as the primary internal and external point of contact for assigned studies; leads cross-functional study teams in executing against protocol requirements, project timelines, and quality standards; escalates issues and risks to the Associate Director or designee in a timely manner.
Proactively identifies potential study risks and contributes to the development and implementation of mitigation actions; communicates findings to the Associate Director or designee and relevant internal stakeholders.
Supports user acceptance testing (UAT) and build specification reviews for applicable systems and platforms used in assigned studies; documents findings and escalates issues to the Associate Director or designee and relevant internal teams as needed.
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