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Coordinate clinical technology validation studies, leading operational planning and day-to-day management of research execution.
Manage subject recruitment and study goals. Determine effective strategies for recruiting and/ or retaining participants.
Serve as primary contact with research participants, vendors, and research leads. Coordinate studies from startup through close-out.
Develop and manage data collection processes. Maintain research project databases, develop trackers, flow sheets and other relevant study documentation.
Maintain research schedules, communicate study milestones and reporting to research team.
Assist research team with Institutional Review Board (IRB) submission and compliance management.
Align operational aspects of research with the needs of other internal stakeholders including engineering, legal, and product requirements.
Assist research team with the assessment and implementation of new best practices and / or processes to gain efficiencies for study set up and administration.
Minimum qualifications
Bachelor's degree or higher in an area requiring significant human subjects research.
5+ years of experience with clinical research in either academic and/or commercial settings, with demonstrated experience in the study lifecycle and clinical research ecosystem.
Track record building successful relationships with Contract Research Organizations (CROs), understanding human subjects needs and clinical research in digital health.
In-depth subject matter knowledge in study start-up, maintenance and closeout, human subjects enrollment, consenting, data collection and data management.
5+ years of experience working with multidisciplinary stakeholders such as research scientists, statisticians, product managers, software engineers.