Clinical Research Coordinator I - Pediatrics Gastroenterology

Washington University in St. Louis

St. Louis (MO)

Vor Ort

USD 28.000 - 39.000

Vollzeit

Vor 4 Tagen

Sei unter den ersten Bewerbenden

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Zusammenfassung

Washington University in St. Louis is seeking a Research Coordinator for a complex observational MOM study focused on infant gut microbiome development.

The role involves coordinating the study, promoting smooth operations, and ensuring IRB/IACUC compliance while engaging with clinical staff and participants. Responsibilities include obtaining informed consent, conducting visits, data entry, and assisting with lab procedures.

Qualifikationen

Bachelor's degree or equivalent experience.
Basic Life Support certification required.
No specific work experience required.

Aufgaben

Coordinate all phases of the study and ensure regulatory compliance.
Recruit and enroll study participants and obtain informed consent.
Conduct study visits in hospital and participant homes and enter data.
Assist with lab procedures and communicate with staff across departments.

Kenntnisse

Clinical Research

Communication

Interpersonal Communication

Organizing

Research

Computer Systems

Ausbildung

Bachelor's degree

Tools

REDCap

Excel

EPIC

Jobbeschreibung

Location

SAINT LOUIS, MO 63110

Scheduled Hours

Position Summary

The Holtz lab is seeking help with a complex observational clinical study 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.

In this position, you will coordinate a complex clinical research study; serve as a resource to provide comprehensive information to clinical staff by promoting a smooth operation, prepare regulatory compliance and interact with other departments.

You will work closely with other team members and healthcare professionals to recruit and enroll study participants, explain the purpose of study and obtain informed consent from participants, conduct study visits in the hospital and the participant's home, ensure compliance with protocol guidelines and requirements of the IRB and IACUC, enter data, and assist with lab procedures.

Preferred applicants are detail orientated, clear communicators, able to provide their own transportation to study visits, curious, enthusiastic, have a flexible schedule (availability needed some weekends, evenings, and early mornings), and have experience with REDCap, Excel, and EPIC.

You may be responsible for multiple research studies simultaneously.

Job Description

Primary Duties & Responsibilities

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 to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.

Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.

Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient's timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.

Collects clinical data under clinical research protocols.

Performs other duties as assigned.

Working Conditions

Job Location/Working Conditions

Patient care setting.

Physical Effort

Typically sitting at desk or table.

Equipment

Office equipment.

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications

Education

Bachelor's degree or combination of education and/or experience may substitute for minimum education.

Certifications /Professional Licenses

The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.

Basic Life Support - American Heart Association, Basic Life Support - American Red Cross

Work Experience

No specific work experience is required for this position.

Skills

Not Applicable

Driver's License

A driver's license is not required for this position.

More About This Job

Required Qualifications

Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).

Preferred Qualifications