Clinical Research Coordinator (Contract)

<p><span style="font-size: 12pt;">Noom is on a mission to help people live better, longer. We’re a consumer-led digital health company, connecting people to content, coaching, community, and clinicians, to build lasting habits and live healthier lives. We’re a high-growth organization powered by science, technology, and world-class talent. When you join Noom, on any team, you’ll see the impact of your work on the world.</span></p> <h2><span style="font-size: 12pt;"><strong>Our Clinical Research Team</strong></span></h2> <p><span style="font-size: 12pt;">Noom’s Clinical Research team is at the heart of our evidence-based approach to whole-person health. We design and conduct rigorous studies to evaluate the effectiveness of our programs and interventions, shaping the future of digital health through science. By aligning clinical integrity with strategic goals, our team ensures Noom's offerings are both credible and transformative.</span></p> <h2><span style="font-size: 12pt;"><strong>About the Role</strong></span></h2> <p><span style="font-size: 12pt;">As Noom continues to expand its research initiatives, we are seeking a <strong>Clinical Research Study Coordinator (Contract)</strong> to support the execution of high-quality clinical research studies. In this hourly contract role, you will play a critical part in the day-to-day coordination and operational management of research studies, ensuring protocol adherence, regulatory compliance, and high-quality data collection.</span></p> <p><span style="font-size: 12pt;">You will partner closely with Clinical Research leadership, cross-functional stakeholders, and external partners to support study start-up, participant engagement, data tracking, and ongoing study operations. You may also help support the execution of User Research (UXR) initiatives.</span></p> <p><span style="font-size: 12pt;">This is a contract, hourly position with flexible remote work within the United States.</span></p> <h2><span style="font-size: 12pt;"><strong>You Will</strong></span></h2> <ul> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Coordinate day-to-day operations of clinical research studies from start-up through close-out</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Support study start-up activities, including documentation preparation, site coordination (if applicable), and regulatory submissions (e.g., IRB materials, amendments, renewals)</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Manage participant recruitment, screening, enrollment, scheduling, and follow-up communications</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Maintain accurate and timely study documentation, including regulatory binders and trial master files</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Ensure protocol adherence and proactively identify and resolve protocol deviations</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Track study milestones, timelines, and deliverables, escalating risks or blockers as needed</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Coordinate data collection processes and ensure high-quality data entry and management</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Serve as a point of contact for participants, ensuring a positive and compliant research experience</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Recruit participants, set up surveys, and provide support as needed for UXR projects</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Collaborate cross-functionally with Product, Data, Clinical Operations, and external vendors to support seamless study execution</span></li> <li style="font-size: 12pt;"><span style="font-size: 12pt;">Contribute to the development and refinement of SOPs and operational workflows for future studies</span><br><br></li> </ul> <h ... (truncated, view full listing at source)