Research Compliance Analyst II

University of California

Los Angeles, CA

JOB DETAILS
SALARY
$31.51–$62.64 Per Hour
SKILLS
Adobe Product Family, Analysis Skills, Clinical Research, Communication Skills, Foundation Grants, Interpersonal Skills, Microsoft Excel, Microsoft Product Family, Organizational Skills, Regulations, Safety Process, Team Player, Time Management
LOCATION
Los Angeles, CA
POSTED
30+ days ago

Research Compliance Analyst II - - 30115 - UCLA Health

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Research Compliance Analyst II

General Information

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Work Location: Los Angeles, CA, USA

Onsite or Remote

Flexible Hybrid

Work Schedule

Monday through Friday, 8:00am to 5:00pm

Posted Date

04/28/2026

Salary Range: $31.51 - 62.64 Hourly

Employment Type

2 - Staff: Career

Duration

Indefinite

Job #

30029

Primary Duties and Responsibilities

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This position coordinates regulatory activities for clinical research studies across assigned units, departments, or divisions. The incumbent conducts detailed reviews of clinical research protocols and prepares, manages, and submits all required regulatory documents and applications to meet UCLA, FDA, sponsor, and other regulatory requirements. The role works closely with study monitors to collect, review, and maintain regulatory documentation, ensuring timely submissions and full compliance with federal, state, and university regulations.

The full salary range for this position is $31.51 - $62.64 per hour.

The budgeted salary range that the university expects to pay $31.51 - $36.00 per hour.

Job Qualifications

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Required:

  • Minimum of 1+ years of experience as a clinical researcher

  • 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.

  • Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.

  • 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.

Preferred:

  • Bachelors degree

As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.

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