Clinical Research Coordinator, Health and Wellbeing

The Health Health and Wellbeing Team at Meta is seeking a Clinical Research Coordinator to support clinical operations. This role will work with a robust team of multidisciplinary stakeholders to support planning and execution of multiple levels of research and validation of novel approaches. The appropriate candidate will manage multiple aspects of research including aligning internal stakeholders (i.e. research teams, engineering, legal) and external partners (i.e. vendors, academic collaborators, IRB, regulators) to deliver results and achieve concrete research and product goals.

Clinical Research Coordinator, Health and Wellbeing 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.
• Travel at least 30%.

• 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.

• In-depth technical experience in digital health and wearable technologies.
• Familiar with software and hardware tooling, electronic data capturing systems that support clinical research studies.