<p>A day in the life…</p> <p>Wondering what a day in the life of a Clinical Research Nurse at Innovo Research might look like?</p> <ul> <li>Deliver direct clinical care to trial participants, including phlebotomy, vital signs, diagnostic testing, and other protocol-required procedures within scope of license. </li><li>Conduct health assessments under investigator oversight to evaluate general health and help assess, manage, and resolve adverse events and safety concerns. </li><li>Manage multiple concurrent trials by supporting screening, recruiting, enrollment, scheduling, study visits, and follow-up while keeping source documentation accurate and audit-ready. </li><li>Monitor, document, and promptly report adverse events and any change in participant status to the Principal Investigator and study team. </li><li>Administer study interventions and treatments (as appropriate), and prepare/monitor investigational products to ensure correct administration, accountability, and documentation. </li><li>Collect, process, and ship laboratory specimens; coordinate protocol procedures and ensure supplies and equipment are ready for each visit. </li><li>Support regulatory and data workflows by completing data entry/query resolution, assisting with IRB submissions and reportable events, following SOPs, and helping train new site staff on study requirements. </li></ul> <p>This job might be for you if you have…</p> <p>Qualifications</p> <ul> <li>Current RN or LPN licensure in the state of employment, with an active nursing license in good standing. </li><li>Associate Degree in Nursing (ADN) from an accredited school of nursing; BLS required. </li><li>Three or more years of experience in a health-related clinic and/or research setting (clinical trials experience preferred). </li><li>Strong organization and documentation skills, with the ability to multitask, manage competing priorities, and maintain exceptional attention to detail. </li><li>Proficiency with Microsoft Office and comfort using clinical/office systems; understanding of medical terminology. </li><li>Ability to build effective working relationships with physicians, coworkers, managers, sponsors/monitors, and clients while practicing integrity and maintaining confidentiality. </li></ul> <p>Bonus points if…</p> <ul> <li>You hold (or are working toward) a clinical research certification such as CCRC. </li><li>You have hands-on experience with investigational product administration/accountability and protocol-driven treatments. </li><li>You enjoy coordinating complex visit schedules across multiple studies and thrive in a fast-paced clinical environment. </li></ul> <p>This role is in-person at a site-specific clinic location; standard schedule is 40 hours/week, with occasional evenings/weekends as needed.</p>