| || 47434BR |
| || Adult CF Registry Coordinator |
| || 9336 Assistant Clinical Research Coordinator |
| || TBD |
| || Medicine / Pulmonary |
| || TBD |
| || Days |
| || Other |
| || JOB OVERVIEW
Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Adult CF Registry 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.
The Adult CF Registry Coordinator 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; and attend team meetings.
Please note: This is a 40% limited appointment starting from the date of hire.
PULMONARY, CRITICAL CARE, ALLERGY AND SLEEP MEDICINE DIVISION
The mission of the Pulmonary, Critical Care, Allergy and Sleep Medicine Division is to be a leader in the provision of comprehensive medical care to patients with pulmonary disease, critical illness, allergic diseases and sleep disorders, to be an engine for innovative research aimed at elucidating basic mechanisms of disease, to translate our research activities into new clinical initiatives, and to provide a rich training environment for the next generation of international leaders in basic, translational and clinical research.
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.
| || • HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
• Proficiency with Microsoft Word, PowerPoint, and Windows. Excel is required
• Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
• 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
Note: Physical/health screening (TB test only), fingerprinting and background check required. Effective March 13, 2017, all final candidate(s) for employment are required to undergo a background check.
| || • 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
| || n/a |
| || Part Time |
| || 40% |
| || The University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. |