University of California, San Francisco
Clinical Research Coordinator - GI Division
University of California, San Francisco, San Francisco, California, United States, 94199
Clinical Research Coordinator - GI Division
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Clinical Research Coordinator - GI Division
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University of California, San Francisco
Job Summary: The Clinical Research Coordinator (CRC) will join the GI Division and responsibilities will include coordination of clinical research studies related to liver disease and liver transplantation. The CRC will perform independently at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigators (PIs). The incumbent will collaborate with Dr. Bilal Hameed and Dr. Bruce Wang on separate research studies.
Duties may include: management and coordination of multiple clinical research studies; act as intermediary between services and departments while overseeing data and specimen management; manage and report study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs; manage investigator’s protocols in the Committee on Human Research online system; participate in review and writing of protocols for institutional review board approval; ensure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in internal and external audits or reviews of study protocols; and perform other duties as assigned.
Salary range: $34.32 - $55.19 (Hourly Rate). For more about benefits, visit https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html.
Required Qualifications:
HS graduation and sufficient experience and demonstrated skills to perform duties.
Attention to detail; strong interpersonal skills; excellent verbal and written communication; ability to multi-task in a fast-paced environment.
Ability to work independently, complete projects timely, and prioritize multiple tasks.
Preferred Qualifications:
BA/BS degree in physical or biological sciences and one year of clinical research experience, or a combination of experience and education.
Fluency in using the Committee of Human Research (CHR) online iMEDris system.
Understanding of patient population to create rapport and realistic participation.
Experience with electronic medical records.
Knowledge of UCSF policies for reimbursement, research guidelines, confidentiality and HIPAA regulations.
Knowledge of medical terminology, research policies, packing/shipping infectious substances, and database building/analysis with Access, Stata, SASS/SPSS, Teleform, etc.
Experience applying Good Clinical Practice Guidelines, HIPAA, protection of human research subjects, CHR regulations, cash handling, environmental health, and fire safety training.
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.
Seniority level: Not Applicable Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Higher Education
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Clinical Research Coordinator - GI Division
role at
University of California, San Francisco
Job Summary: The Clinical Research Coordinator (CRC) will join the GI Division and responsibilities will include coordination of clinical research studies related to liver disease and liver transplantation. The CRC will perform independently at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigators (PIs). The incumbent will collaborate with Dr. Bilal Hameed and Dr. Bruce Wang on separate research studies.
Duties may include: management and coordination of multiple clinical research studies; act as intermediary between services and departments while overseeing data and specimen management; manage and report study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs; manage investigator’s protocols in the Committee on Human Research online system; participate in review and writing of protocols for institutional review board approval; ensure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in internal and external audits or reviews of study protocols; and perform other duties as assigned.
Salary range: $34.32 - $55.19 (Hourly Rate). For more about benefits, visit https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html.
Required Qualifications:
HS graduation and sufficient experience and demonstrated skills to perform duties.
Attention to detail; strong interpersonal skills; excellent verbal and written communication; ability to multi-task in a fast-paced environment.
Ability to work independently, complete projects timely, and prioritize multiple tasks.
Preferred Qualifications:
BA/BS degree in physical or biological sciences and one year of clinical research experience, or a combination of experience and education.
Fluency in using the Committee of Human Research (CHR) online iMEDris system.
Understanding of patient population to create rapport and realistic participation.
Experience with electronic medical records.
Knowledge of UCSF policies for reimbursement, research guidelines, confidentiality and HIPAA regulations.
Knowledge of medical terminology, research policies, packing/shipping infectious substances, and database building/analysis with Access, Stata, SASS/SPSS, Teleform, etc.
Experience applying Good Clinical Practice Guidelines, HIPAA, protection of human research subjects, CHR regulations, cash handling, environmental health, and fire safety training.
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.
Seniority level: Not Applicable Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Higher Education
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