• Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV). • Participate in the site selection process with oversight from the Clinical Team Lead role. • Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved. • Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials. • Provide mentoring, training, and co-monitoring of junior clinical team members. • Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements. • Attend and present at meetings and conferences, including Investigator Meetings. • Participate in the RFP process, including business development meetings. • Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials. • Perform both onsite & remote monitoring and study closure activities across multiple protocols.

• Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV). • Participate in the site selection process with oversight from the Clinical Team Lead role. • Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved. • Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials. • Provide mentoring, training, and co-monitoring of junior clinical team members. • Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements. • Attend and present at meetings and conferences, including Investigator Meetings. • Participate in the RFP process, including business development meetings. • Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials. • Perform both onsite & remote monitoring and study closure activities across multiple protocols.

• Conducting thorough research into an individuals’ background using a variety of tools, such as databases and public records • Gathering information, analyzing data, and compiling this information to be entered into a final report • Processing searches related to background screening reports • Ensuring all searches are processed and reported according to state and federal laws as outlined in AccuSourceHR’s reporting guidelines • Ensuring all searches are processed according to client guidelines • Retrieving public records information and entering said information into our platform • Analyzing information and comparing data sets to confirm matching identifiers • Performing other duties as assigned • Meeting or exceeding minimum standard service requirements

Role Description The Research Study Coordinator will lead day-to-day operations to support a NIDA-funded SBIR grant studying telehealth buprenorphine treatment across five high-risk settings. This is a grant-funded, two-year position with a defined end date. In this role, you will manage: - Site coordination - Participant-facing research activities, including a targeted recruitment push for study participants - Survey data management What You’ll Do - Site Coordination & Operations - 40% - Serve as the primary day-to-day point of contact for all five partner sites - Monitor study progress, timelines, and site-level recruitment milestones; proactively identify and troubleshoot barriers - Participate in and document monthly site operations calls - Refresh study site staff on study protocol, informed consent procedures, and REDCap data entry if needed - Manage IRB submissions (e.g. amendments, renewals, and adverse event documentation) under the supervision of the Senior Research Associate - Patient Participant Recruitment, Follow-Up & Stipends - 40% - Coordinate with site referral pipelines to maintain rolling patient participant recruitment - Screen participants for eligibility and conduct informed consent across all five sites - Complete REDCap enrollment and baseline data entry - Conduct proactive follow-up outreach with enrolled participants at 4, 8, 12, and 16 weeks after enrollment for survey completion - Administer phone-based assessments when web-based responses are not received - Track follow-up completion rates by site and flag gaps to the Senior Research Associate - Issue and track participant stipends via ClinCard at each assessment timepoint across all five sites - Coordinate smartphone device ordering, deployment, and participant troubleshooting across all five sites - Data Management - 20% - Enter and maintain all participant data in REDCap with a high degree of accuracy - Prepare and submit data exports to UMass Chan Medical School (biostatistics partner) on schedule - Conduct regular data quality checks in collaboration with Boulder’s Data Director - Assist with scheduling participant qualitative interviews after 16-week follow-up completion; coordinate delivery of completed recordings to transcription vendor Qualifications - 2 years of experience in clinical or public health research coordination, or equivalent experience in a related social services or community health role - Master’s degree in social science, public health, or a related field - Familiarity with IRB processes and Good Clinical Practice (GCP) principles - Comfort with remote work, virtual collaboration tools, and high-volume outreach via phone and email - Deep commitment to harm reduction and improving the health and dignity of people who use drugs Nice to Have - Experience working in a startup or fast-paced, high-growth environment - Experience with REDCap or similar electronic data capture platforms - Familiarity with NIH grant processes including progress reports (RPPRs) Supervisory Responsibility This position has no supervisory responsibilities. Work Environment This is a fully remote role but we are currently only hiring candidates located in the following states: - AZ - CA - CO - FL - GA - ID - IL - KY - MA - NC - NJ - NY - OH - OR - PA - SC - TN - TX - UT - WA - WV Applicants must reside and work in one of those states to be considered. Expected Hours This is a full-time, grant-funded position at 100% FTE, with Pacific hours mandatory. Team members may work with their managers to adjust work hours within this timezone to suit the needs of the position. Team members may be asked to work additional days as work demands require. Travel Approximately 5% travel is expected. Travel includes site visits to partner sites in Washington, Oregon, and Ohio to support study start-up, staff training, and ongoing implementation monitoring. Travel is planned and coordinated in advance; all travel costs are covered by the grant. Compensation The starting pay range for this position is $65,000-70,000 annually; base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including equity grants in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave). Perks & Benefits - Contribute to meaningful, life-saving work! - Comprehensive medical, dental, vision, and short-term disability benefits designed to take care of our employees and their families - Mental Health Services via insurance coverage, including Talkspace and EAP for continuous care - Supplemental mental health services through Talkspace for care needed following tough patient visits - 4 weeks of vacation accrued per calendar year with a tenured increase to 5 weeks at 2 years of employment - Sick leave accrued at 1 hr for every 30 hrs paid - 9 Paid Holidays per year - 12 weeks of 100% paid parental leave for the birth or adoption of a child (after 6 months of employment) - 401(k) retirement savings - Remote friendly with hardware provided to complete your work duties Our Values - The people we care for always come first - Our opportunity is also our duty, in service to others - Share facts to change minds, instill empathy to change hearts - Move the industry forward: follow the data - Strong individuals, stronger together Hiring Process As part of our hiring process, all final candidates will be required to undergo background checks and provide professional references. By applying, you acknowledge and consent to these checks, which may include employment history, criminal records, education/licensing verification, and professional references. We are committed to transparency and confidentiality throughout this process and will inform you in advance should any further information be required. Boulder Care believes the people who manage our product and team should be representative of those who use the platform. This includes people from backgrounds that are historically underrepresented in the industry. We celebrate differences and are committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, citizenship, marital status, disability, gender identity, or veteran status. If you are a qualified person with a passion for what we do, please apply!