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Assistant Clinical Research Coordinator - Hematology​/Oncology; Santa Monica

Job in Santa Monica, Los Angeles County, California, 90403, USA
Listing for: UCLA Health
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Assistant/Associate
Salary/Wage Range or Industry Benchmark: 27.08 - 43.55 USD Hourly USD 27.08 43.55 HOUR
Job Description & How to Apply Below
Position: Assistant Clinical Research Coordinator - Hematology/Oncology (Santa Monica)

Work Location: Santa Monica, CA, USA

Onsite or Remote

Flexible Hybrid

Work Schedule

Monday – Friday, 8:00am - 5:00pm

Posted Date

01/29/2026

Salary Range
: $27.08 - 43.55 Hourly

Employment Type

Duration:
Indefinite

Job # 28474

Primary Duties and Responsibilities

The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. In this role, you will perform necessary tasks to assist in managing projects and prioritizing work to meet necessary deadlines. You will provide support in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations.

The full hourly salary range for this position is $28.43- $45.73

Job Qualifications

Required:

  • Minimum of 1+ years of experience in a clinical research setting
  • Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.
  • Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
  • Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
  • Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
  • Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
  • Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines.
  • High degree of concentration and focus in a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual.
  • Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc.

Preferred

  • Bachelor’s Degree in related area and/or equivalent combination of education and experience.
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