Clinical Research Coordinator I - Neurology

Overview The clinical research coordinator’s position focuses on industry-sponsored clinical trials at the John L. Trotter Multiple Sclerosis Center. The coordinator will work in the lab of Dr. Rob Naismith, Professor of Neurology, and with a clinical trial research team. This role supports MS patients and participates in studies sponsored by NIH, Department of Defense, National MS Society, and pharmaceutical companies. For more information on the center’s research, visit: . For information on MS, visit: Primary Duties & Responsibilities Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and regulatory requirements; establishes record-keeping systems; assesses participants\' progress; analyzes, investigates and reports adverse events; decides when to notify physicians, stop participant inclusion, or adjust protocols; resolves protocol management issues and advises on corrective action; liaises with funding or sponsoring agencies. Recruits and enrolls study participants; determines eligibility; develops informed consent packets and explains study purpose to participants; administers and scores tests and evaluates lab and clinical assessments to ensure timely completion. Ensures timely completion of protocol requirements (assessments, lab testing, procedures, and treatments); evaluates and interprets clinical data; prepares presentations or reports on progress trends and provides conclusions and recommendations. Collects clinical data under clinical research protocols. Performs other duties as assigned. Working Conditions Patient care setting Typically sitting at a desk or table Office equipment Education, Certifications & Qualifications Education: Bachelor’s degree or equivalent combination of education and experience acceptable for minimum requirements. Certifications/Professional Licenses: Basic Life Support (BLS) from American Heart Association or American Red Cross. Certification must be obtained within one month of hire date. Work Experience: No specific work experience required. Skills: Not Applicable Driver's License: Not required. More About This Job & Qualifications Preferred Qualifications: Prior experience with industry-sponsored clinical trials; strong communication, detail orientation; experience conducting informed consent discussions; hands-on experience with ECGs, blood draws, and lab processing. Benefits & Salary Grade: C09 Salary Range: $47,400.00 - $71,200.00 / annually Benefits include vacation, holidays, sick time, health insurance, transit pass, and retirement savings (403(b)). EEO & About WashU EEO Statement: Washington University in St. Louis is committed to equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information. Compliance & Application Info Pre-Employment Screening: All external candidates offered employment will undergo required screenings, including background checks, drug screen, and verification of education/licensure where applicable. All offers are contingent upon successful completion of required screening. For accommodations in applying, contact View email address on click.appcast.io. #J-18808-Ljbffr Washington University in St. Louis