Assistant Clinical Research Coordinator at University of… · San…

Summary: The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research and excellence in patient care. They are seeking an Assistant Clinical Research Coordinator to support and coordinate clinical studies, assist with data collection and analysis, and ensure compliance with study protocols. Responsibilities: - Perform entry-level duties related to the support and coordination of clinical studies - May be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials - Help prepare protocols for study initiation - Help design flow sheets, data forms and source documents - Gather and interpret medical, surgical and laboratory data regarding clinical trial subjects - May apply understanding of inclusion/exclusion eligibility criteria for protocols - Help recruit, enroll, register, schedule and retain study subjects - Record protocol specific treatments and assure collection and shipment of samples - Assist research personnel to keep patients on study schedules - Complete study forms to submit to sponsors and/or appropriate agencies - Collect, enter and clean data into study databases, maintaining data quality - Assist with data analysis - Assist with preparation of reports and tables - Attend team meetings - Perform other duties as assigned Required Qualifications: - HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training - Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team - Attention to details - Proficiency with Microsoft Word, PowerPoint, and Windows - Excellent analytical and problem-solving skills - Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects - Ability to establish cooperative working relationships with patients, co-workers, & physicians Preferred Qualifications: - Demonstrated proficiency with medical terminology - Experience working with patients or study subjects - Ability to abstract data from medical records and transfer it to data collection forms or directly into databases Required Skills: Clinical trial coordination, Data collection, analysis Important Skills: Microsoft Word, Microsoft PowerPoint Nice-to-Have Skills: Medical terminology, Patient interaction, communication skills, Organizational skills, Interpersonal skills, Attention to detail, Problem-solving skills, Project management