Wilmington, NC30+ days ago
Responsibilities: • Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling) • Prepare lab kits for each subject based on study protocols • Ship biological specimens following IATA guidelines and protocol requirements • Maintain specimen logs, shipping records, temperature logs, and other documentation • Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests) • Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups • Clean and sanitize lab equipment and work areas daily • Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA) • Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs • Respond to and resolve electronic data queries • Verify accuracy and completeness of data entries and study documentation • Participate in quality control and assurance initiatives to ensure regulatory compliance • Monitor and maintain inventory of lab kits and supplies • Order dry ice and other lab necessities • Destroy expired kits and log per protocol • Support preparation of study-specific training materials and lab manuals • Collaborate with study coordinators and medical staff to meet visit protocol requirements • May assist with infusion monitoring under clinician supervision. • Previous experience in clinical research is a huge plus • Proficient with Microsoft Office (Excel, Outlook, Word) and database systems • Must be comfortable with performing Research Assistant tasks when the lab is slow • Ability to handle potentially hazardous materials safely • Strong organizational, time management, and multitasking skills • Excellent verbal and written communication; strong interpersonal skills • Ability to work independently and as part of a cross-functional team • Customer-service mindset and high level of professionalism.