Clinical Research Coordinator I
Location: San Francisco California
Description: University of California San Francisco is at present recruited Clinical Research Coordinator I right now, this job will be placed in California. For complete informations about this job opportunity kindly see the descriptions. Under the supervision of the Manager of Research Personnel/Nurse Educator, Clinical Research Coordinators (CRC I) support the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and/or other types of consortium trials for one of multiple oncology programs as assigned/needed. Responsibilities include managing protocols and tasks assigned by the Lead Research Coordinator and/or the Faculty Leader of the Program to ensure study initiation is completed before enrolling subjects, compliance of protocol management occurs based on regulations, and safety of subjects is maintained. The incumbent enters accurate subject and trial data into the HDFCCC OnCore® CTMS in order to run reports for adverse events and accrual as required. The incumbent can support 4-6 active studies and 4-6 follow-up studies, depending on the complexity of the patients and procedures. Independently, the CRC I maintains protocol files, subject source records, and enters and cleans protocol data for each assigned study. The incumbent supports the investigator in research study project management to assure compliance with the Code of Federal Regulations and the ICH Guidance on Good Clinical (Research) Practice as well as UCSF Institutional policies. The incumbent also supports the research team with additional duties as assigned by the Lead CRC and/or the Faculty Leader; will also perform other duties as assigned. Note: There are multiple openings. Required Qualifications B.A. or B.S. with a major in science or related field and one year of experience in administrative analysis or operations research; or an equivalent combination of education and experience; research writing skills; prior experience with various computer programs, like Microsoft Office; experience with internet database entry using specialized software such as Oncore; knowledge and experience in managing oncology clinical trials; ability to sit and work at a computer for several hours per day; may need to travel between one or more campuses via UCSF shuttle; knowledge of federal, state and local research regulations and guidelines involving human subject research; proven ability to balance multiple projects and meet deadlines by managing 2-3 protocols in prior positions; able to communicate medical terminology verbally and in writing; knowledge of Microsoft Office, database management. Physical Demands: requires bending, squatting, climbing stairs, reaching up to shoulder height; pushing/pulling up to and above 60 pounds; reaching above shoulder level; sitting, standing, walking, waist twisting, kneeling, crawling; carrying/lifting up to and over 60 pounds; gripping/grasping, fine/gross finger manipulation; repetitive movements of upper and lower extremities; may be exposed to chemical agents; tuberculosis, blood, body fluids or tissue, and radiological materials; latex, dust, fumes or gases; loud noises; differentiate color; use protective equipment; operate vehicle.
Note: Fingerprinting and background check required. Preferred Qualifications Two-three years experience; UCSF IRB data system of experience; familiarity with UCSF research and oncology unit policies and procedures; Membership in a clinical research professional society.
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This job starts available on: Sun, 29 Jul 2012 10:59:47 GMT