Clinical Research Coordinator - Semel Institute

General Information

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Work Location: Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday-Friday 8am-5pm Posted Date 03/07/2025 Salary Range: $33.63 - 54.11 Hourly Employment Type 2 - Staff: Career Duration indefinte Job # 23026

Primary Duties and Responsibilities

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The Semel Institute is seeking to hire a full time Clinical Research Coordinator (CRC) who will contribute to the overall operational management of clinical research / trial / study activities from design to closeout. You will be responsible for the implementation of research activities for one or more studies. In this role you will recognize and perform necessary tasks to manage projects and prioritizes work to meet necessary deadlines. You are also responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). Collaboration with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies including, but not limited to, compliant conduct, financial management, and adequate personnel support is also essential to this role. 

Pay Range: $33.63 - $54.11 hourly

Job Qualifications

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• Bachelors Degree or 2+ years of previous study coordination or clinical research coordination experience 
• 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, 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.
• Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
• Organization skills to create and maintain administrative and regulatory files effectively as well as indepe