ClinicalResearchCoordinator

👋 Meet knownwell https://www.knownwell.co/, weight-inclusive healthcare for all. Join a dynamic company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it.   Backed by $50M in funding—including a $25M round led by CVS Health Ventures with support from a16z Bio + Health, Flare Capital, MassMutual, and Intermountain Ventures—we’re scaling fast and expanding access to evidence-based obesity care nationwide.   🔍 The Clinical Research Coordinator (CRC) is responsible for overseeing and coordinating all aspects of clinical trials, ensuring that studies are conducted in compliance with regulatory requirements, sponsor expectations, and Good Clinical Practice (GCP) guidelines. The CRC will act as the primary liaison between the clinical research team, patients, and external stakeholders, ensuring the efficient and timely execution of clinical research projects.    Location: Schaumburg, IL  On-site Requirements: Hybrid, mostly on-site.     *knownwell does not offer relocation assistance* 🎯 What you'll do: - Study Coordination:  - Coordinate and manage all aspects of clinical trials, including patient recruitment, screening, and enrollment.  - Schedule and oversee patient visits, ensuring timely collection of data and samples in accordance with the study protocol.  - Oversee site initiation, monitoring, closeout activities, and equipment calibration to ensure compliance with study protocols and regulations.  - Maintain study documentation, including case report forms, consent forms, and other essential study records.  - Review monitoring follow-up letters to ensure timely completion and resolution of identified issues.  - Ensure accurate and timely reporting of adverse events (AEs) and serious adverse events (SAEs).  - Manage the receipt, shipment, and storage of study drug and tria