No experience
Employment Type:
Full time
Job Category:
Health Care Provider
Health Care & Medicine
Public Administration Analyst
(This job is no longer available)
UCLA Health | Los Angeles, CA
Grad Date

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Job Description

Job Duties
Coordinate research activities related to HIV clinical trials. Responsible for assigned start up and closure of clinical research studies, patient registration, randomization, compliance, patient recruitment, enrollment, data management and education as related to the protocol. Document symptoms and other changes for reporting to PI as appropriate with research patients. Assist in report preparation for IRB, GCRC and other regulatory agencies and/or committees. Participate in quality assurance. Interact with study monitors regarding protocol management and resolution of study queries. Work with fund manager for budgeting and billing of studies.

Job Qualifications
Demonstrated ability to audit and analyze data for completeness and accuracy. Ability to maintain records and follow-up on protocol patients. Ability to work efficiently and complete tasks with a high degree of accuracy. Ability to work and solve problems with minimal supervision. Ability to prioritize effectively. Ability to work flexible hours to complete tasks and meet deadlines. Ability to concentrate and focus on tasks in a work environment that contains distracting stimuli. Ability to be flexible in handling work delegated by more than one individual. Strong interpersonal communication skills effectively and diplomatically interact with others. Strong written and verbal communication skills. Typing & computer skill/ability including word-processing, use of spreadsheet, e-mail, and data entry. Ability to supervise clinician assistant as associated with specific protocol management and implementation. Working knowledge and previous experience with clinical trials, data management and case report forms. Knowledge of medical terminology and lab procedures. Familiarity with AIDS symptoms and HIV medications. Knowledge and experience of working with regulatory agencies, i.e., IRB, GCRC and other regulatory agencies and/or communities. Working experience of the start-up and closure of clinical research studies and patient registration and randomization. Working knowledge and understanding of AMC and ACTG policies, protocols and CRF completion. Preferred: Verbally bilingual in English and Spanish. Current phlebotomy certification. Bachelor's or Masters in Social Science or Health.

About UCLA Health

For more than half a century, UCLA Health  has provided the best in healthcare and the latest in medical technology to thepeople of Los Angeles and throughout the world. Today we are one of the most comprehensive and advanced healthcare systems in existence. We are comprised of Ronald Reagan UCLA Medical Center, UCLA Medical Center, Santa Monica, Resnick Neuropsychiatric Hospital at UCLA, Mattel Children’s Hospital UCLA, and the UCLA Medical Group, with offices throughout the region.

Ronald Reagan UCLA Medical Center is consistently ranked by U.S.News & World Report as one of the top five hospitals in the nation and the best medical center in the western United States. The doctors, scientists and caregivers of UCLA are leaders in their fields. Every day, they perform pioneering work across an astounding range of disciplines, from organ transplantation and cardiac surgery to neurosurgery and cancer treatment. Year after year, our people have achieved medical breakthroughs and earned the highest industry honors. And we’re just getting started.

The dedicated professionals of UCLA Health are committed to healing humankind, one patient at a time, by improving health, alleviating suffering, and delivering acts of kindness on a daily basis.