Clinical Research Coordinator I (Data) - Neurology

Position Summary Assists investigators as a data coordinator of clinical research trials of all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it into an Electronic Data Capture (EDC). May be responsible for numerous research trials simultaneously. Helps ensure the accurate collection of study‑required procedures while patients are receiving protocol treatment and are in active protocol follow‑up. Scheduled Hours 40 hours per week. Job Description Primary Duties & Responsibilities Works under the Principal Investigator’s guidance to meet the research objectives of the project. Assists with study start‑up activities including IRB applications for initial review, modifications/amendments, continuing reviews, and reportable events. Works with research team to identify, screen, and enroll study subjects. Ensures protocol requirements are met, including but not limited to direct contact with research participants; collection of basic health information; coordination of study‑related procedures; handling, processing, and shipping of research specimens; organization of source documentation and data entry. Prepares/submits reportable event reports to sponsor(s), IRB and regulatory agencies in accordance with the study protocol and established policies, procedures, and regulations. Collaborates with sponsor’s research associates during monitoring activities by providing study documentation, data clarifications, and reports, as necessary. Performs other duties incidental to the work described above. Working Conditions Normal office environment. Typically sitting at a desk or table; standing or walking; bending, crouching, stooping. Office equipment. Education & Training Bachelor’s degree or combination of education and/or experience may substitute for minimum education. Basic Life Support certification required within one month of hire date. (Optional: SOCRA/ACRP certification.) No additional work experience required. Skills Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Interpersonal Communication, Organizing, Research Support. Driver's License Not required. Grade & Salary Grade: C09 Salary Range: $47,400.00 – $71,200.00 per annum. Benefits Statement Up to 22 days of vacation, 10 recognized holidays, and sick time. Competitive health insurance packages, priority appointments, lower copays/coinsurance. Free Metro transit U‑Pass for eligible employees. Defined contribution (403(b)) Retirement Savings Plan, employee and university contributions starting at 7%. Wellness challenges, annual health screenings, mental health resources, mindfulness programs, employee assistance program (EAP), financial resources, access to dietitians. 4 weeks of caregiver leave to bond with new child. Family care resources for ongoing childcare needs. WashU covers cost of tuition for employees and families: 100% of WashU undergraduate tuition and 40% elsewhere after seven years. EEO Statement Washington University in St. Louis is committed to the principles and practices of 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, age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information. #J-18808-Ljbffr Washington University in St. Louis