The David Geffen School of Medicine (DGSOM), Department of Urology is seeking to hire a full-time Qualitative Research Coordinator to join the Population-Health Research Core (PHRC). The ideal candidate for this role will have a strong background in research methodology and study coordination and logistics. This position presents an exciting opportunity to be part of a fast-paced team responsible for providing the A-Zs of population health research--development, implementation, and dissemination... more details
General Information
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Work Location: Los Angeles, USA
Onsite or Remote
Fixed Hybrid
Work Schedule
M-F; 8am-5pm; Hours May Vary
Posted Date
05/07/2024
Salary Range: $24.28 - 48.04 Hourly
Employment Type
2 - Staff: Career
Duration
indefinite
Job #
16282
Primary Duties and Responsibilities
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The David Geffen School of Medicine (DGSOM), Department of Urology is seeking to hire a full-time Qualitative Research Coordinator to join the Population-Health Research Core (PHRC). The ideal candidate for this role will have a strong background in research methodology and study coordination and logistics. This position presents an exciting opportunity to be part of a fast-paced team responsible for providing the A-Zs of population health research--development, implementation, and dissemination. Under the direction of the PHRC Manager, the Qualitative Research Coordinator will work across various departments with a variety of personnel and leading health care researchers (i.e., Principal Investigators, Sub-Investigators, trainees, and national/international collaborators) to complete the following duties:
Serve as a subject-matter resource in qualitative research methodologies to guide and assist in the development of qualitative research studies
Assist in the development of applications to be submitted to the appropriate regulatory bodies (i.e., IRBs)
Assure compliance with all aspects of individual studies ensuring that protocols are completed accurately, safely, and in a timely manner
Be responsible for research assessment and study participant intervention under the supervision of the Principal Investigator
Be responsible for relevant regulatory and research practice guidelines
Work with the PI to refine study protocols and procedures, as needed
Participate in patient recruitment and enrollment, data collection, source documentation, quality assurance, regulatory submissions of events as needed, and protocol dissemination to required study participants.
Facilitate and participate in regular meetings with the study team to provide updates on research progress
Pay Range: $24.28 - $48.04 Hourly
Job Qualifications
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Bachelor’s Degree required. Master’s in health science field, such as nursing, public health, biology, etc. preferred.
Minimum of one year of research experience.
Bi-lingual (English/Spanish) – skill in speaking clearly, distinctly, and using appropriate vocabulary and grammar to obtain and convey information. Required only for specific positions.
Demonstrated population health-based research experience, with basic knowledge of subject matter, including working knowledge of good clinical practices for clinical research.
Demonstrated knowledge and experience in conducting individual qualitative interviews, focus groups, development of interview and focus group guides, analysis of qualitative data using ATLAS.ti and/or Dedoose.
Ability to work efficiently and complete tasks with a high degree of accuracy.
Demonstrated organizational skills to handle multiple research projects for efficiency and cost-effectiveness, including handling work delegated by more than one individual.
Experience in performing study participant enrollment, eligibility evaluations and interventions under the direction of the Principal Investigator with diverse population using strong experience and skills, as assigned.
Analytical skills to analyze information, practices, and procedures. Formulate logical and objective conclusions and make recommendations for effective solutions.
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