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Clinical Research Coordinator - Rheumatology

UCLA Health
Fixed HybridRemotefull_timeVerifiedPosted 9 Oct 2024
💰 $108,000/yr($66,000/yr$108,000/yr)

About the role

General Information

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Work Location: Los Angeles, USA Onsite or Remote Fixed Hybrid Work Schedule Monday- Friday 8am-5pm Posted Date 10/08/2024 Salary Range: $33.63 - 54.11 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 19458

Primary Duties and Responsibilities

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The Clinical Research Coordinator at UCLA Health plays a vital role in managing all aspects of clinical research studies, from initial design and setup to conduct and closeout. This position is responsible for implementing research activities across one or more studies, ensuring strict adherence to study protocols, institutional policies, FDA regulations, and ICH Good Clinical Practice guidelines. You will manage projects, prioritize tasks, and ensure that all research activities are completed on time and within scope. Collaboration with Principal Investigators, ancillary departments, sponsors, and central research teams is key to supporting the administration of studies, including regulatory compliance, financial management, and staffing. Join UCLA Health and contribute to advancing clinical research in a dynamic and innovative environment.

Salary: $33.63 - $54.11 hourly

Job Qualifications

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Required:

  • 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.

Preferred:

  • Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
  •  Working knowledge of the clinical research regulatory framework and institutional requirements.
  • 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.
  • Fluent in writing and speaking Spanish.

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Company

UCLA Health

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