University of California, San Francisco
Clinical Research Coordinator
University of California, San Francisco, San Francisco, California, United States, 94199
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Clinical Research Coordinator
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University of California, San Francisco The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit, specifically for Genitourinary Oncology program; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Department
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is the only cancer center in the Bay Area to receive the prestigious designation of “comprehensive” from the National Cancer Institute. We combine basic science, clinical research, epidemiology, cancer control and patient care throughout UCSF. Currently, the HDFCCC conducts over 700 clinical trials across various departments. Job Summary
The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit, specifically for Genitourinary Oncology program; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Responsibilities Support the management and coordination of single or multiple clinical research studies, depending on size and complexity. Act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results. Create, clean, update, and manage databases and comprehensive datasets and reports. Coordinate staff work schedules; assist with training of Assistant CRCs and other CRC team members. Assist the Research Personnel Manager and/or PI with oversight of other research staff; help ensure compliance with relevant regulatory agencies. Oversee study data integrity; implement and maintain periodic quality control procedures. Interface with departments to obtain UCSF approvals prior to study initiation; maintain regulatory documents in partnership with the Regulatory department. Report study progress to investigators; participate in internal and external audits or reviews of study protocols; perform other duties as assigned. Salary and Benefits
The final salary and offer components are subject to additional approvals based on UC policy. Placement within the salary range depends on work experience and internal equity. For positions represented by a labor union, placement is guided by the collective bargaining agreement. Salary range:
$34.32 - $55.19
per hour. For benefits information, visit:
https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html Required Qualifications High school graduation and sufficient experience and demonstrated skills to perform duties. Attention to detail; strong interpersonal and communication skills; ability to multi-task in a fast-paced environment; ability to coordinate with subjects, team members, other departments, and outside institutions. Ability to work independently, complete projects timely, and prioritize multiple tasks to meet deadlines. Knowledge and understanding of research, especially in biological sciences. Experience with computer programs (Microsoft Office; internet-based databases) and specialized software such as OnCore. Ability to sit and work at a computer for several hours; may need to travel between UCSF campuses; ability to stand for several hours. Experience in clinical research or related training; familiarity with specimen processing. Working knowledge of federal, state, and local research regulations and guidelines; knowledge of research practices in laboratory or clinical settings. Ability to interpret and apply policies; respond to requests; resolve issues; work in a team-oriented environment. Ability to work with oncology patients and handle sensitive population needs. Preferred Qualifications Analytical and writing skills in a science/research environment. Fluency with CHR online iMEDris system for protocol submissions, renewals, and modifications. Understanding of patient population to foster rapport and appropriate participation. Experience with electronic medical records. Knowledge of UCSF policies on reimbursement, confidentiality, HIPAA, and patient safety; familiarity with medical terminology and data management tools (Access, Stata, SPSS, Teleform). Knowledge of clinical research in breast oncology and oncology trial management. Membership in a clinical research professional society. Experience applying Good Clinical Practice (GCP), HIPAA, and CHR regulations related to recruitment, consent, and safety. About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through research, education, and patient care. It is dedicated exclusively to the health sciences. We are committed to equity and PRIDE values ( professionalism, respect, integrity, diversity and excellence ). 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. Job Details
Location: San Francisco, CA; Campus: Mission Bay (SF); Employment type: Full-time; Work Style: Flexible; Shift: Days; Shift Length: 8 Hours; Additional Shift Details: Monday - Friday.
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Clinical Research Coordinator
role at
University of California, San Francisco The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit, specifically for Genitourinary Oncology program; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Department
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is the only cancer center in the Bay Area to receive the prestigious designation of “comprehensive” from the National Cancer Institute. We combine basic science, clinical research, epidemiology, cancer control and patient care throughout UCSF. Currently, the HDFCCC conducts over 700 clinical trials across various departments. Job Summary
The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit, specifically for Genitourinary Oncology program; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Responsibilities Support the management and coordination of single or multiple clinical research studies, depending on size and complexity. Act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results. Create, clean, update, and manage databases and comprehensive datasets and reports. Coordinate staff work schedules; assist with training of Assistant CRCs and other CRC team members. Assist the Research Personnel Manager and/or PI with oversight of other research staff; help ensure compliance with relevant regulatory agencies. Oversee study data integrity; implement and maintain periodic quality control procedures. Interface with departments to obtain UCSF approvals prior to study initiation; maintain regulatory documents in partnership with the Regulatory department. Report study progress to investigators; participate in internal and external audits or reviews of study protocols; perform other duties as assigned. Salary and Benefits
The final salary and offer components are subject to additional approvals based on UC policy. Placement within the salary range depends on work experience and internal equity. For positions represented by a labor union, placement is guided by the collective bargaining agreement. Salary range:
$34.32 - $55.19
per hour. For benefits information, visit:
https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html Required Qualifications High school graduation and sufficient experience and demonstrated skills to perform duties. Attention to detail; strong interpersonal and communication skills; ability to multi-task in a fast-paced environment; ability to coordinate with subjects, team members, other departments, and outside institutions. Ability to work independently, complete projects timely, and prioritize multiple tasks to meet deadlines. Knowledge and understanding of research, especially in biological sciences. Experience with computer programs (Microsoft Office; internet-based databases) and specialized software such as OnCore. Ability to sit and work at a computer for several hours; may need to travel between UCSF campuses; ability to stand for several hours. Experience in clinical research or related training; familiarity with specimen processing. Working knowledge of federal, state, and local research regulations and guidelines; knowledge of research practices in laboratory or clinical settings. Ability to interpret and apply policies; respond to requests; resolve issues; work in a team-oriented environment. Ability to work with oncology patients and handle sensitive population needs. Preferred Qualifications Analytical and writing skills in a science/research environment. Fluency with CHR online iMEDris system for protocol submissions, renewals, and modifications. Understanding of patient population to foster rapport and appropriate participation. Experience with electronic medical records. Knowledge of UCSF policies on reimbursement, confidentiality, HIPAA, and patient safety; familiarity with medical terminology and data management tools (Access, Stata, SPSS, Teleform). Knowledge of clinical research in breast oncology and oncology trial management. Membership in a clinical research professional society. Experience applying Good Clinical Practice (GCP), HIPAA, and CHR regulations related to recruitment, consent, and safety. About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through research, education, and patient care. It is dedicated exclusively to the health sciences. We are committed to equity and PRIDE values ( professionalism, respect, integrity, diversity and excellence ). 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. Job Details
Location: San Francisco, CA; Campus: Mission Bay (SF); Employment type: Full-time; Work Style: Flexible; Shift: Days; Shift Length: 8 Hours; Additional Shift Details: Monday - Friday.
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