DescriptionClinical Research Supervisor provides immediate supervision to routineresearch study coordination. Individual supervises unit operations to ensurecompliance with departmental and organizational policies, procedures, anddefined internal controls. Supervises operational management of clinicalresearch/trial/study activities from design, set up, conduct, through closeout.The Clinical Research Supervisor oversees planning and organizing necessarytasks to ensure adherence to the study protocol and applicable regulations,such as institutional policy and procedures, FDA Code of Federal Regulations(CFR), and ICH Good Clinical Practice (GCP). Serves as liaison with thePrincipal Investigator (PI), ancillary departments, central researchinfrastructure teams, sponsors, institutions, and other entities as needed tosupport the administration of all aspects of studies, including, but notlimited to, compliant conduct, financial management, and adequate personnelsupport. The responsibilities outlined in the job description provide a generaloverview of duties and tasks performed the role. Performance of duties andtasks will vary based on the department operations, the type of study and scopeof service.Salary Range: $78800.00 - $175000.00 AnnuallyQualificationsRequired:
Bachelor's degree required, Master's degree preferred.
Minimum of 5+ years of experience in a clinical research setting.
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.
Ability to effectively communicate to and interact with patients in a compassionate and kind manner.
Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines.
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.)
Preferred:
Clinical Research Certification (CCRP, ACRP, etc.)
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