Assistant Study Coordinator (LAUNCH Program)

General Information

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Work Location: Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday-Friday, 8:00am-5:00pm Posted Date 05/28/2025 Salary Range: $27.08 - 43.55 Hourly Employment Type 4 - Staff: Limited Duration 12-Months Job # 23610

Primary Duties and Responsibilities

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As the Assistant Study Coordinator for the LAUNCH program, you will assist 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 recognize and perform necessary tasks to assist the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in managing projects and prioritizing work to meet necessary deadlines. You will support the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations. The full salary range for this position is $27.08 - $43.55/Hourly. The budgeted salary that the University reasonably expects to pay for this position is $27.08/Hourly.

This is one of six open positions. By applying to this posting, you’ll be considered for all available opportunities. 

Please note that this is a full-time 12-month limited position and may convert to career.

Salary Range: $27.08 - $43.55/Hourly

Job Qualifications

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Required:

• Minimum of 1+ years of experience in a clinical research setting.
• Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators, and administration and to work as a member of a team.
• Ability to effectively communicate to and interact with patients in a compassionate and kind manner.
• Ability to set priorities and complete ongoing tasks with competing deadlines 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 requirement