Clinical Research Coordinator Job at UCLA Health
The Division of Pulmonary Medicine is seeking a motivated Clinical Research Coordinator to implement a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository. In this role, you will closely collaborate with the Principal Investigator (PI) of each study, to facilitate timely study progress reporting to the PI and enabling appropriate PI oversight, study management, including development of source worksheets and documents, safe and accurate completion of protocol required procedures in accordance with standard operating procedures, governing regulations and study documents, and perform drug accountability, patient management, including recruitment, patient interfacing, enrollment, and scheduling, and regulatory management. You will work with Principal Investigators, Sub-Investigators, support staff, federal and state agencies, industry partners, and other collaborative departments to coordinate and manage investigator-initiated and sponsor-initiated clinical trials and research endeavors.
Target hourly salary: $24.28-$48.04
- Demonstrated working knowledge of current medical terminology to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms.
- Clinical research experience, with in depth knowledge of respective therapeutic area as it pertains to clinical trials and studies.
- Demonstrated knowledge of “good clinical practices” for clinical research as defined by ICH and FDA.
- Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.
- Demonstrated ability to prioritize workload to meet demands of PI’s, Sponsor and FDA.
- Demonstrated interpersonal skills to work with patients, their families/ guardians, physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a
- Demonstrated English verbal skills to obtain and convey accurate information, explaining research protocol to patients and other staff.
- Ability to work at more than one site, travel to participating clinics and attend off-site staff meetings, conferences and investigators meetings.
- A bachelor’s degree in Science or related fields.
- Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management…etc.
UCLA 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, disability, or protected Veteran status.
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