New

Clinical Research Coordinator

University of California - San Francisco
$38.23-$61.48
United States, California, San Francisco
1 Daniel Burnham Court (Show on map)
Apr 07, 2026
As a Clinical Research Coordinator, you will execute, manage, and coordinate a research protocol for a study assessing the effects of a cutting-edge, novel therapeutic on adolescent and young adults with mental health conditions, including young people with eating disorders. You will lead study protocol piloting/execution, recruitment, participant interaction, data collection, and data/project management efforts. Your duties may include managing and reporting on study progress; overseeing study data integrity; implementing and maintaining regular quality control procedures; and performing other duties as assigned. Required qualifications: HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred qualifications: Spanish fluency. CPT-1 or equivalent licensure to perform venipuncture. One to two (1-2) years of experience as a Clinical Research Coordinator or related role. Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. Experience in a community or medical setting or working with research study participants. Prior experience with clinical research: recruiting, collecting data, data entry, and good clinical practice. Familiarity with regulatory directives. Prior experience with screening, interviewing, eliciting informed consent, scheduling and explaining study requirements to participants in clinical research studies. Project and/or data management experience. Experience with electronic medical records. Experience with RedCap. Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines Health Information and Accountability Act (HIPAA) The Protection of Human Research Subjects CHR regulations for recruitment and consent of research subjects Experience working with adolescents and/or young adults with eating disorders. 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. 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. 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. Salary Information The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html Required qualifications: HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred qualifications: Spanish fluency. CPT-1 or equivalent licensure to perform venipuncture. One to two (1-2) years of experience as a Clinical Research Coordinator or related role. Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. Experience in a community or medical setting or working with research study participants. Prior experience with clinical research: recruiting, collecting data, data entry, and good clinical practice. Familiarity with regulatory directives. Prior experience with screening, interviewing, eliciting informed consent, scheduling and explaining study requirements to participants in clinical research studies. Project and/or data management experience. Experience with electronic medical records. Experience with RedCap. Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines Health Information and Accountability Act (HIPAA) The Protection of Human Research Subjects CHR regulations for recruitment and consent of research subjects Experience working with adolescents and/or young adults with eating disorders.