Remote Regulatory Compliance Lead - Clinical Research

UCLA Health

Los Angeles (CA)

Remote

USD 77,000 - 160,000

Full time

14 days+

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Job summary

UCLA Jonsson Comprehensive Cancer Center, part of UCLA Health, seeks a regulatory coordinator to ensure compliance for complex clinical research studies. You will manage regulatory submissions, maintain documentation, and collaborate with monitors for timely study activation and ongoing oversight.

The role requires 3+ years in clinical research coordination, strong communication, and proficiency with Adobe and Excel.

Qualifications

  • Minimum of 3+ years of clinical research coordination experience.
  • Ability to communicate professionally and work in a team.
  • Ability to manage priorities and meet deadlines while adhering to policies and regulations.
  • Analytical skills to assess protocols and regulatory requirements.
  • Attention to detail in a fast-paced environment.
  • Organizational skills to maintain regulatory files and deadlines.
  • Proficiency with Adobe and Microsoft Office, especially Excel.
  • Willingness to learn new tools and processes quickly.
  • Knowledge of clinical research concepts, policies and safety regulations.
  • Experience with IRBs and regulatory committees.

Responsibilities

  • Review protocols and prepare regulatory documents for UCLA, FDA, NCI, IRB and sponsors.
  • Maintain complete regulatory files and ensure timely collection of essential documents.
  • Collaborate with study monitors to ensure compliance with laws and policies.
  • Audit and monitor interventional trials overseen by DSMB.
  • Review external monitoring/audit reports and track follow-up actions.
  • Maintain and update the Clinical Trial Database for reporting.
  • Interpret regulations and communicate expectations to study teams.
  • Review patient eligibility for DSMB-monitored studies.

Skills

Regulatory coordination
Communication
Prioritization
Analytical thinking
Attention to detail
Organization
Adobe/Excel proficiency
Learning mindset
Clinical research knowledge
IRB processes understanding

Education

Bachelor's degree or equivalent

Tools

Adobe Acrobat
Microsoft Office (Excel)

Job description

UCLA Jonsson Comprehensive Cancer Center, part of UCLA Health, seeks a regulatory coordinator to ensure compliance for complex clinical research studies. You will manage regulatory submissions, maintain documentation, and collaborate with monitors for timely study activation and ongoing oversight.

The role requires 3+ years in clinical research coordination, strong communication, and proficiency with Adobe and Excel.

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