Assistant Clinical Research Coordinator - Ophthalmology

General Information

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Work Location: Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday-Friday 8am-5pm Posted Date 01/08/2025 Salary Range: $27.08 - 43.55 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 21592

Primary Duties and Responsibilities

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The Assistant Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the coordination of research activities for one or more studies. The incumbent recognizes and performs necessary tasks to coordinate projects and prioritizes work to meet necessary deadlines. The incumbent participates in 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). The Study Coordinator collaborates 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. The responsibilities outlined in the job description provide a general overview of duties and tasks performed by Clinical Research Coordinators. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service. 

Job Qualifications

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All 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, 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.

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