Epi Research Coordinator 1 Grant - Chicago, United States - RUSH University Medical Center
Description
Location:
Chicago, IL
Hospital:
RUSH University Medical Center
Department:
Rush Alzheimers Dis Ctr-ResFac
Work Type:
Full Time (Total FTE between 0. 9 and 1. 0)
Shift:
Shift 1
Work Schedule:8 Hr (8:00:00 AM - 4:30:00 PM)
Travel Required:
reliable transportation and valid driver's license needed
Bilingual with Spanish and English is not required, but a great skill set to have
Summary:
The EPI Research Coordinator 1 coordinates Epidemiological, Behavioral or Human Translational, or Population Health research studies and performs a variety of duties including the collection compilation and documentation of research data.
The Coordinator 1 partners with other members of the research team to ensure the research is conducted in accordance with the study protocol, local, state, and federal guidelines related to epidemiologic/ behavioral/ translational research.
Exemplifies the Rush mission, vision and ICARE values and acts in accordance with Rush policies and procedures.Other information:
Required Job Qualifications:
Bachelor's Degree in related field.
Two years general research experience with two years working on Human Subjects research.
Demonstrate knowledge of Good Epidemiological Practice (GEP) and/or Good Clinical Practice (GCP).
Strong organizational skills.
Demonstrates basic computer skills.
Strong written and verbal communication skills.
Ability to collaborate within multi-disciplinary team settings.
May require personal transportation to field location depending on assignment.
Ability to work independently.
Ability to develop and maintain effective relationships with a variety of stakeholders.
Availability to work evenings, overnight and weekends if called for under the study protocols.
Responsibilities:
- Coordinates aspects of less complex research studies including, but not limited to, study start-up, initiation activities, participant recruitment, enrollment, completion of data collection, maintenance of data integrity, and study close-out.
- Assists with the development of study related Standard Operating Procedures for new study protocols.
- May assist in the collection of study data both through interviews and collecting samples or testing results as described by the study protocol.
- May assist with preliminary data organization and/or guided analysis.
- Primary participant contact for all study related questions and issues.
- May help coordinate study team workload and training schedules to ensure optimal use of resources.
- Follows Federal and Rush guidelines in the collection of study data and other study related activities.
- Troubleshoots field issues when necessary. Uses discretion to resolve issues when unplanned events arise.
- May assist with Institutional Review Board (IRB) assignments such as initial study approval, amendments, continuing reviews and updating study documents for IRB approval.
- May assist PI with aspects of grant proposals.
- May act as lead for less experienced Research Assistants, work-study students, interns and volunteers including orientation, training, and providing performance feedback.
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