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Form of workThis is a part-time position (40 hours per two week pay period), with day shifts, primarily Monday through Friday.
Join the Scripps Health team and work alongside passionate caregivers and provide patient-centered healthcare. Receive endless appreciation while you build a rewarding career with one of the most respected healthcare organizations nationwide.
Why join Scripps Health?
AWARD-WINNING WORKPLACE:
#5 in Fortune Best Workplaces in Health Care 2023
#78 in 2023 PEOPLE Companies that Care
#95 in Fortune 100 Best Companies to Work for 2023
Recognized by Newsweek as one of America's Greatest Workplaces for Diversity in 2024
Nearly a quarter of our employees have been with Scripps Health for over 10 years.
Why join this team?
Join Scripps Memorial La Jolla Trauma Administration Team as a Trauma Research Associate. You'll be able to work hand-in-hand with the trauma team and contribute to studies and truly make a change. The Trauma Research Associate supports the Trauma Research Director and Data Quality Coordinator with all research related activities including:
Development of IRB approved Trauma Research, pilot studies and performance improvement (PI) projects.
Assists with maintenance and oversight of all data quality of the Trauma Registry including development of reports and related analyses for the Trauma Service and those necessary for epidemiologic research.
Assists with preparation of all required data to San Diego County and national trauma databases.
Assists with documentation and follow-up of all utilization of the trauma registry database, including data requests for research or performance improvement projects.
Assists with management of all IRB studies, including development and maintenance.
Responsible for management of all human subjects training certification for all research staff, including notification of renewals and new training.
Supportive role with all injury prevention strategy development and outreach efforts.
Must be able to work independently, demonstrating dedication, high productivity, analytical skills, critical thinking and self-management in a fast-paced environment while meeting strict deadlines.
Required Qualifications:
BS or BA required.
Prefer 2 years of experience with IRB approved research, including sponsored clinical trials.
Knowledge of AAAM injury severity coding is highly desirable.
Understanding and experience with epidemiologic methodology and study design, data collection and GCP (Good Clinical Practice) guidelines.
Demonstrate ability to work collaboratively and communicate effectively.
Excellent written and oral English skills coupled with expert grammatical and proof reading skills.
High level proficiency with data analysis presentation through basic statistical analyses, graphing and tables.
High level proficiency with Microsoft Excel and PowerPoint. Proficient with Microsoft Office Suite, Endnote, Adobe, and scientific software.
Completion of AAAM coding and trauma registrar coursework within one year of employment.
Certification in trauma registry (CSTR) within 2 years.
Preferred Qualifications:
Masters Level in public health, biostatistics or epidemiology.
Certification in clinical research (CCRP, CCRC, CRC).
Knowledge and experience with the National Trauma Database (NTDB), Trauma Quality Improvement Program (TQIP), ISS (Injury Severity Scoring) AIS (Anatomical Injury Scaling) and AAAM (Association of Automotive Medicine) coding conventions.
