Clinical Research Coordinator - Commuity Health Research
Clinical Research Coordinator - Commuity Health Research
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$ 34 - 55
1 Vacancy
Job Description
The Clinical Research Coordinator (CRC) will work independently to execute manage and implement clinical research protocols with guidance from an experienced Clinical Research Director and faculty scientists with an outstanding track record in research productivity and mentoring and CRCs duties may include but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies (e.g. surgical trials novel precision therapies lifestyle interventions population health and correlative science). To support individual studies the CRC will lead on participant screening and enrollment data and specimen collection and management; data entry and quality control; and regular reporting to the Clinical Research Director and faculty investigator team. The CRC may be involved in the creation and management of databases datasets or reports to support the research enterprise. The CRC may coordinate staff work schedules and assist with training of Assistant CRCs. The CRC may act as intermediary between scientific teams and cores that may span departments or units and assist the Clinical Research Director and/or PI with oversight of other research staff. The CRC will manage study protocols in the Committee on Human Research (CHR) online system (Institutional Review Board IRB) and assist with development or modification of study protocols. The CRC will help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; and participate in any internal and external audits or reviews of study protocols.
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.
The salary range for this position is $34.32 $55.19 (Hourly Rate).
To learn more about the benefits of working at UCSF including total compensation please visit: graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/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.
Department Description
The Clinical Research Coordinator (CRC) will work independently to execute manage and implement clinical research protocols with guidance from an experienced Clinical Research Director and faculty scientists with an outstanding track record in research productivity and mentoring and CRCs duties may include but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies (e.g. surgical trials novel precision therapies lifestyle interventions population health and correlative science). To support individual studies the CRC will lead on participant screening and enrollment data and specimen collection and management; data entry and quality control; and regular reporting to the Clinical Research Director and faculty investigator team. The CRC may be involved in the creation and management of databases datasets or reports to support the research enterprise. The CRC may coordinate staff work schedules and assist with training of Assistant CRCs. The CRC may act as intermediary between scientific teams and cores that may span departments or units and assist the Clinical Research Director and/or PI with oversight of other research staff. The CRC will manage study protocols in the Committee on Human Research (CHR) online system (Institutional Review Board IRB) and assist with development or modification of study protocols. The CRC will help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; and participate in any internal and external audits or reviews of study protocols.
About UCSF
The University of California San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research graduatelevel education in the life sciences and health professions and excellence in patient care. It is the only campus in the 10campus UC system dedicated exclusively to the health sciences. We bring together the worlds 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 at
Join us to find a rewarding career contributing to improving healthcare worldwide.
Required Experience:
IC
Employment Type
Full Time
