UCLA Health
Clinical Research Supervisor
UCLA Health, Los Angeles, California, United States, 90079
Description
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
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
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.
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
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
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.