Clinical Research Coordinator: Trials & Compliance

UCLA Health; Los Angeles (CA); On-site; USD 43,000 - 68,000; Full time

Job summary

UCLA Health in Los Angeles seeks an Assistant Clinical Research Coordinator to manage trial coordination from setup through closeout. You will collaborate with the PI, departments, and sponsors to ensure compliant conduct and timely task execution.

The role emphasizes regulatory compliance, data integrity, and effective communication with patients and staff, with a strong focus on meeting study deadlines.

Qualifications

• 1+ years of experience in a clinical research setting.
• Ability to communicate professionally with students, staff, and collaborators.
• Ability to interact compassionately with patients.
• Ability to prioritize tasks and meet deadlines under regulations.
• Analytical skills to assess protocols and regulatory requirements.
• Attention to detail in a fast-paced environment.
• Organizational skills to maintain regulatory files.
• Proficiency with Adobe and Microsoft suite, especially Excel.
• Willingness to learn new tools and processes.
• Knowledge of local IRBs and regulatory bodies.

Responsibilities

• Coordinate research activities for multiple studies from design to closeout.
• Plan tasks to ensure study protocol adherence and regulatory compliance.
• Collaborate with PI, departments, sponsors, and teams to support administration of studies.
• Ensure compliant conduct, financial management, and staff support.

Skills

Clinical research

IRB experience

Communication

Regulatory compliance

Excel

Team collaboration

Adobe

Microsoft Office

Education

Bachelor’s Degree

Tools

Adobe

Microsoft Office

Excel

Job description

UCLA Health in Los Angeles seeks an Assistant Clinical Research Coordinator to manage trial coordination from setup through closeout. You will collaborate with the PI, departments, and sponsors to ensure compliant conduct and timely task execution.

The role emphasizes regulatory compliance, data integrity, and effective communication with patients and staff, with a strong focus on meeting study deadlines.