Clinical Research Coordinator

Clinical Research Coordinator

Location: Burlingame, CA

Job Type: Fulltime

Responsibilities

• 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.
• Travel at least 30%.