Research Study Coordinator

<p><strong>About Boulder</strong></p> <p>Boulder Care is an award-winning digital clinic for addiction medicine, recognized for both innovation and high quality of patient care. Founded in 2017 by CEO Stephanie Strong, our mission is to improve the lives of people with substance use disorders through compassionate, evidence-based care.</p> <p>We provide Boulder patients with a fully virtual, multidisciplinary care team—including medical providers and peer recovery specialists—who deliver personalized treatment, including medication for opioid use disorder (MOUD) and ongoing support. Our approach is grounded in clinical excellence, patient-centered care, and a commitment to reducing barriers to recovery. Boulder partners with leading health plans, employers, and community organizations to ensure that our services are accessible and covered for the people who need them most.</p> <p>Named by Fortune as one of the Best Workplaces in Healthcare, we foster a culture of kindness, respect, and meaningful work that delivers outstanding patient outcomes and moves the addiction medicine industry forward.</p> <p><strong>About this Role</strong></p> <p>The <strong>Research Study Coordinator</strong> will lead day-to-day operations to support a NIDA-funded SBIR grant studying telehealth buprenorphine treatment across five high-risk settings. <strong>This is a grant-funded, two-year position with a defined end date.</strong> In this role, you will manage site coordination, participant-facing research activities—including a targeted recruitment push for study participants—and survey data management.</p> <p><strong>What You’ll Do&nbsp;</strong></p> <p><strong>Site Coordination &amp; Operations - 40%</strong></p> <ul> <li>Serve as the primary day-to-day point of contact for all five partner sites</li> <li>Monitor study progress, timelines, and site-level recruitment milestones; proactively identify and troubleshoot barriers</li> <li>Participate in and document monthly site operations calls</li> <li>Refresh study site staff on study protocol, informed consent procedures, and REDCap data entry if needed</li> <li>Manage IRB submissions (e.g. amendments, renewals, and adverse event documentation) under the supervision of the Senior Research Associate</li> </ul> <p><strong>Patient Participant Recruitment, Follow-Up &amp; Stipends - 40%</strong></p> <ul> <li>Coordinate with site referral pipelines to maintain rolling patient participant recruitment</li> <li>As needed via phone—Screen participants for eligibility and conduct informed consent across all five sites</li> <li>As needed via phone—Complete REDCap enrollment and baseline data entry</li> <li>Co