Jobs and Careers
WA
Clinical Research Coordinator II - Pediatrics GI
Washington University in St. LouisNorthwest Towerfull_timeVerifiedPosted 4 Sept 2024
💰 $78,900/yr($52,600/yr – $78,900/yr)
About the role
Scheduled Hours
40Position Summary
We are seeking help with two ongoing observational clinical studies at Washington University School of Medicine.The Maternal Offspring Microbiome (MOM) study aims to understand how the infant gut is first populated with bacteria and viruses. We are interested in defining if babies obtain their microbiome from their environment, from the people who care for them, or from their pets.
Our study on pediatric celiac disease progression is a multisite study which aims to understand immune system signals, active genes in the small intestine, and small intestinal and stool microbial communities which allow loss of gluten tolerance and tissue injury.
In this position, you will recruit and enroll study participants, explain the purpose of study and obtain informed consent from participants, conduct study visits at the medical center and the participant’s home, ensure compliance with protocol guidelines and requirements of the IRB, enter data, assist with lab procedures, perform data analyses, and help with manuscript and grant preparation.
Preferred applicants are detail orientated, clear communicators, manage time effectively, able to provide their own transportation to study visits, curious, enthusiastic, have experience with REDCap, Excel, and EPIC.
Job Description
Primary Duties & Responsibilities:
- Confers with PI to assist in developing plans for research projects and discuss the interpretation of results.
- Collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies.
- Assists in the preparation of amendments to protocols and/or modifications to study design as appropriate.
- Coordinates the development of forms, questionnaires, and the application of research techniques.
- Assists in writing instructional procedure manuals for study progress, data collection and coding.
- Reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
- Routinely implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
- Establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates, and reports adverse events.
- Makes decisions as when to notify PI of issues, when to stop participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants.
- Resolves IRB/protocol management issues and recommends corrective action as appropriate.
- Evaluates and interprets collected clinical data in conjunction with PI as appropriate.
- Prepares oral or written presentations of reports and analyses setting forth progress trends and provides recommendations or conclusions.
Working Conditions:
Job Location/Working Conditions
Patient care setting
Physical Effort
Typically sitting at desk or table
Equipment
Office equipment
Required Qualifications
Education:
Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Certifications:
Work Experience:
Skills:
Driver's License:
More About This Job
Required Qualifications
- Basic Life Support certification (Online Basic Life Support certifications, those without a skills assessment component, are not sufficient to meet the Basic Life Support requirements).
Preferred Qualifications
Education:
No additional education beyond what is stated in the Required Qualifications section.
Certifications:
Work Experience:
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