Clinical Research Coordinator, CARE Center

2 weeks ago

Los Angeles, United States UCLA Health Full time

General Information

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Work Location: Los Angeles, USA

Work Schedule

Monday - Friday, 8:00am - 5:00pm

Posted Date

12/04/2023

Salary Range: $32.65 - 52.53 Hourly

Employment Type

2 - Staff: Career

Duration

Indefinite

Job #

3073

Primary Duties and Responsibilities

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As the Clinical Research Coordinator for the Department of Medicine, CARE Center, you will be responsible for performing research activities directly related to HIV clinical trials and COVID-19 clinical trials. Duties include:

* Coordinate activities for clinical research studies, such as participant recruitment and enrollment; data management; and education as related to each protocol
* Document signs, symptoms and other changes with research patients
* Assist with preparing reports and submissions
* Participate in quality assurance activities for studies across the research unit
* Work with outreach team in expanding recruitment efforts for COVID-19 and HIV trials

Salary range: $32.65-$52.53 Hourly

Job Qualifications

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Required:

* Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
* Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
* Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
* Ability to be flexible in handling work delegated by more than one individual.
* Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
* Ability to handle confidential material information with judgement and discretion.
* Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
* Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
* Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
* Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
* Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
* Working knowledge of the clinical research regulatory framework and institutional requirements.

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