Job Description

• Deliver direct clinical care to trial participants, including phlebotomy, vital signs, diagnostic testing, and other protocol-required procedures within scope of license. 
• Conduct health assessments under investigator oversight to evaluate general health and help assess, manage, and resolve adverse events and safety concerns. 
• Manage multiple concurrent trials by supporting screening, recruiting, enrollment, scheduling, study visits, and follow-up while keeping source documentation accurate and audit-ready. 
• Monitor, document, and promptly report adverse events and any change in participant status to the Principal Investigator and study team. 
• Administer study interventions and treatments (as appropriate), and prepare/monitor investigational products to ensure correct administration, accountability, and documentation. 
• Collect, process, and ship laboratory specimens; coordinate protocol procedures and ensure supplies and equipment are ready for each visit. 
• 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. 

• Current RN or LPN licensure in the state of employment, with an active nursing license in good standing. 
• Associate Degree in Nursing (ADN) from an accredited school of nursing; BLS required. 
• Three or more years of experience in a health-related clinic and/or research setting (clinical trials experience preferred). 
• Strong organization and documentation skills, with the ability to multitask, manage competing priorities, and maintain exceptional attention to detail. 
• Proficiency with Microsoft Office and comfort using clinical/office systems; understanding of medical terminology. 
• Ability to build effective working relationships with physicians, coworkers, managers, sponsors/monitors, and clients while practicing integrity and maintaining confidentiality. 

• You hold (or are working toward) a clinical research certification such as CCRC. 
• You have hands-on experience with investigational product administration/accountability and protocol-driven treatments. 
• You enjoy coordinating complex visit schedules across multiple studies and thrive in a fast-paced clinical environment.