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General Information

Work Location: Los Angeles, USA
Onsite or Remote
Fixed Hybrid
Work Schedule
Monday through Friday; 8;00am-5:00pm, 3 days on-site minimum.
Posted Date
11/13/2024
Salary Range: $6983.33 - 14950 Monthly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
20687

Primary Duties and Responsibilities

The Clinical Research Supervisor oversees the coordination and management of clinical research studies, ensuring compliance with study protocols, institutional policies, FDA regulations (CFR), and ICH Good Clinical Practice (GCP). This role leads all phases of clinical trials, from design through closeout, and supervises research staff to ensure efficient, compliant operations. The supervisor works closely with Principal Investigators (PIs), central research teams, sponsors, and other stakeholders to support study execution, financial management, and resource allocation. Responsibilities may vary based on study type and departmental needs.

Salary: $6,983.33 - $14,950 per month


Job Qualifications

Required:

  • Bachelor’s degree required
  • Minimum of 5+ years of experience in a clinical research setting
  • 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.
  • Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc…
  • Advanced 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.
  • Demonstrated ability to interpret IRB, FDA, federal and UCLA requirements and utilize that information to guide investigators and other team members
  • Expert level working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws
  • Demonstrated experience and knowledge of clinical trials budgeting processes to manage the preparation of clinical trials budgets
  • Demonstrated experience with FDA processes and procedures.
  • Ability to lead the development and implementation of quality improvement activities, SOPs, processes, etc.
  • Team leadership experience (i.e. projects, committees, etc.).
  • Ability to develop and give presentations to leadership, positively representing the department.
  • Ability to predict potential problems and proactively implement solutions.
  • Ability to clearly communicate complex departmental and institution-wide policies and ensure understanding.
  • Ability to manage complex and sometimes conflicting departmental priorities and external timelines.  

 Preferred:

  • Clinical Research Certification (CCRP, ACRP, etc.)
  • Masters degree

As a condition of employment, the final candidate who accepts a conditional 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; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.