Research Study Coordinator 1 (Temporary)

University of Washington Medical Center•Seattle, WA

1d•$21 - $27

About The Position

The Department of Emergency Medicine has an outstanding opportunity for a Temporary Research Coordinator to participate in clinical research at Harborview Medical Center (HMC). The Research Coordinator will coordinate and perform work in support of clinical and health services research in EMS. Research projects will cover a wide range of clinical pathways with a focus on out-of-hospital cardiac arrest, traumatic injuries, strokes, prehospital whole blood, advanced airway management, and opioids. The research coordinator will work in a team environment that includes faculty, fellows, medical students, and other key stakeholders within Seattle Fire Department and the University of Washington’s Paramedic Training program. This position requires research experience. The team must have confidence in the processes used and the work products of this individual. They also must be able to rely on his/her/their ability to move projects forward with professionalism, accuracy, and timeliness. This individual must have a working knowledge of qualitative and quantitative approaches to data collection, management, analysis, and reporting.

Requirements

Two years of college level course work in a relevant academic area AND two years of experience performing work in support of clinical, biomedical, or behavioral research studies involving human subject.
Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration.

Nice To Haves

Bachelor's Degree in health or science related field
Experience with EFIC Studies
Proficiency in statistical analysis software
Prior EMS experience
Excellent verbal, written, and interpersonal communication skills
Well-honed organizational skills and ability to manage multiple priorities and timelines
Ability to work with colleagues in a way that enhances collaboration and team building
Expert Proficiency in Microsoft Office Suite
Experience with analysis and statistical skills
Experience using REDCap or other database software
Previous experience in a research environment

Responsibilities

Perform data collection and data entry process; prepare summary reports and regular updates and perform periodic quality checks to ensure the integrity of the data collected
Assist with development and maintenance of research databases.
Contribute to development of study protocol and evaluation metrics.
Analyze collected data for accuracy.
Recruit, screen and consent participants or legal representative.
Facilitate timely enrollment of study participants and explanation of research procedures to participants.
Ensure informed consent forms from participants and participant family members have been obtained.
Ensure Federal and State Regulatory compliance including HIPAA.
Actively contribute writing IRB applications/modifications for complex research protocols.
Maintain Institutional Review Board (IRB) approvals and correspondence, including amendments and renewals as necessary in collaboration with Clinical Research Manager.
Serve as primary point of contact for research participant recruitment, scheduling and questions about studies.
Provide project support to keep activities within scope, timeline, and budget; track project milestones and identify opportunities for knowledge sharing.
Prepare and maintain study materials for the Institutional Review Board (IRB).
Draft and edit manuscripts and grant proposals; prepare materials for meetings and workshops.
Complete literature reviews relating to ongoing research.
Serve as research contact for UW research collaborators and outside collaborators.
Attend necessary meetings and conferences for ongoing research projects
Assist with onboarding new hourly Research Assistants as needed