Assistant Clinical Research Coordinator

UCSF•San Francisco, CA

2d•$33 - $54

About The Position

Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Assistant Clinical Research Coordinator will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey-level work at the next level within the series. UCSF’s Division of Pediatric Critical Care is pioneering research across a spectrum of critical health challenges to improve outcomes for the most vulnerable children. Investigators are exploring ways to protect and support the developing brain, studying how to strengthen the blood-brain barrier and improve the delivery of life-saving therapeutics for children with neurological disorders. Other areas of focus include understanding and promoting healthy lung development in preterm infants, with the goal of creating new therapies for chronic lung diseases that arise from premature birth. About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values [https://www.ucsf.edu/about/mission-and-values]. In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here [https://diversity.ucsf.edu/]. Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

Requirements

Entry-level duties related to the support and coordination of clinical studies
Training and development to prepare and advance for journey-level work at the next level within the series

Responsibilities

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