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General Information

Work Location: Los Angeles, USA
Work Schedule
Monday - Friday, 8:00am - 5:00pm
Posted Date
09/27/2024
Salary Range: $33.63 - 54.11 Hourly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
3073

Primary Duties and Responsibilities

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: $33.63-$54.11 Hourly

Job Qualifications

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.