Research Coordinator

Determines protocol-related needs to conduct the trial and orders supplies and equipment Recruits and screens potential patients and obtains informed consent Assists in providing patient education and benefits and risks of participating in a clinical drug trial Designs organizational tools and forms to facilitate accurate data collection and recordkeeping Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol Manages research funds Schedules patient visits and laboratory and diagnostic test procedures Coordinates drug shipments, storage, and accountability with pharmacy Coordinates with Investigational Pharmacy for subjects to receive required drugs Reviews trends, problems encountered, patient adverse events, and patient progress Draws blood or collects other samples as needed and eligible Requirements Bachelor's Degree and research experience required Master's Degree preferred Phlebotomy certification or venipuncture skills preferred BLS HCP certification from AHA preferred Certification in clinical research (SoCRA, ACRP) preferred Core Competencies Demonstrates expertise in clinical trial management, including patient recruitment, informed consent, and data collection. Proficient in coordinating drug shipments and managing research funds while ensuring compliance with clinical research standards. #J-18808-Ljbffr