Clinical Research Coordinator II - Medical Oncology

Position Summary Assists investigators as coordinator of a complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; manages and records all phases of study protocol as required by sponsoring agency to ensure compliance. Scheduled Hours 40 hours per week. Job Description Assists in developing plans for research projects and discusses the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate. Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies. Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record‑keeping systems; makes assessments and determinations of participants’ progress; analyzes, investigates and reports adverse events; makes decisions regarding physician notification, participant inclusion, protocol adjustments and corrective actions; serves as liaison with funding or sponsoring agency. Evaluates and interprets collected clinical data; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions. Performs other duties as assigned. Working Conditions Patient care setting. Typically sitting at desk or table. Equipment: Office equipment. Qualifications Education: Bachelor’s degree or combination of education and/or experience may substitute for minimum education. Certifications/Professional Licenses: Basic Life Support – American Heart Association, Basic Life Support – American Red Cross. Work Experience: Clinical Research (2 Years). Skills: Clinical Research, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis. Driver’s License: Not required for this position. Basic Life Support certification must be obtained within one month of hire date. Online BLS certifications without a skills assessment component do not meet the requirement. Salary Range $54,600.00 – $81,900.00 per year. Benefits Statement Personal: Up to 22 days of vacation, 10 recognized holidays, and sick time. Competitive health insurance packages with priority appointments and lower copays/coinsurance. Free Metro transit U‑Pass for eligible employees. Defined contribution 403(b) retirement savings plan with employee and university contributions starting at 7% (subject to applicable policies). Wellness: Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians. Family: 4 weeks of caregiver leave for bonding with a new child. Family care resources for ongoing childcare needs. Adult care support available. WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us. 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 (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status or genetic information. #J-18808-Ljbffr Washington University in St. Louis