Washington University in St. Louis
Clinical Research Coordinator II (Hybrid) - Psychiatry
Washington University in St. Louis, Washington, Missouri, United States, 64930
Clinical Research Coordinator II
The Department of Psychiatry is seeking a Clinical Research Coordinator II to assist investigators as coordinator of a complex clinical research study. This position may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants, and will manage and record all phases of study protocol as required by sponsoring agency to ensure compliance. Primary Duties & Responsibilities: Recruits, screens, and schedules participants for study per protocol. Obtains informed consent, administers interviews, intervention, and collects urine samples for testing. Assists in training and supervising staff on study procedures including how to administer informed consent, interviews, intervention, and collect urine samples for testing. Responsible for ensuring adherence to recruitment and study protocols and completion of staff assignments. Performs quality control of data collected to ensure it is accurate and provides feedback to research staff. Manages databases for tracking and recruiting research participants and collecting data in REDCap. Monitors monthly productivity goals of research staff and provides detailed reports to Principal Investigator. Assists in completing and maintaining IRB documentation and approval, including consent forms, study instruments, modifications, continuing reviews, and data sharing. Responsible for maintaining adherence to the protocol and maintaining records of any changes to the procedures. Assists Principal Investigator with preparation of reports and slides for meetings, publications, NIH progress reports and NIH grant applications. Manages and oversees purchasing activities, including research study supplies, staff expenditures and research participant payments. Working Conditions: Patient care setting. Clinical office setting with some pressure caused by study deadlines. Physical Effort: Typically sitting at desk or table. Equipment: Office equipment. Required Qualifications: Education: Bachelor's degree or combination of education and/or experience may substitute for minimum education. Certifications: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross. Work Experience: Clinical Research (2 Years). Preferred Qualifications: Prior management experience and human subject research experience. Salary Range: $52,600.00 - $78,900.00 / Annually
The Department of Psychiatry is seeking a Clinical Research Coordinator II to assist investigators as coordinator of a complex clinical research study. This position may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants, and will manage and record all phases of study protocol as required by sponsoring agency to ensure compliance. Primary Duties & Responsibilities: Recruits, screens, and schedules participants for study per protocol. Obtains informed consent, administers interviews, intervention, and collects urine samples for testing. Assists in training and supervising staff on study procedures including how to administer informed consent, interviews, intervention, and collect urine samples for testing. Responsible for ensuring adherence to recruitment and study protocols and completion of staff assignments. Performs quality control of data collected to ensure it is accurate and provides feedback to research staff. Manages databases for tracking and recruiting research participants and collecting data in REDCap. Monitors monthly productivity goals of research staff and provides detailed reports to Principal Investigator. Assists in completing and maintaining IRB documentation and approval, including consent forms, study instruments, modifications, continuing reviews, and data sharing. Responsible for maintaining adherence to the protocol and maintaining records of any changes to the procedures. Assists Principal Investigator with preparation of reports and slides for meetings, publications, NIH progress reports and NIH grant applications. Manages and oversees purchasing activities, including research study supplies, staff expenditures and research participant payments. Working Conditions: Patient care setting. Clinical office setting with some pressure caused by study deadlines. Physical Effort: Typically sitting at desk or table. Equipment: Office equipment. Required Qualifications: Education: Bachelor's degree or combination of education and/or experience may substitute for minimum education. Certifications: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross. Work Experience: Clinical Research (2 Years). Preferred Qualifications: Prior management experience and human subject research experience. Salary Range: $52,600.00 - $78,900.00 / Annually