Clinical Research Coordinator II - Pediatrics Emergency Medicine

Position Summary

Assists investigators as coordinator of basic to complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. This position also requires rotating overnight on-call duties outside of the essential functions, specifically for the duration of an existing trauma trial. Additional compensation for these overnight on-call duties is provided.

Job Description

Primary Duties & Responsibilities:

• 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 physicians 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; serves as liaison with funding or sponsoring agency.
• Primarily recruits and enrolls study participants in a clinical setting. When needed, recruits and enrolls study participants off-site in community settings such as EMS agencies; makes and/or participates in making determinations of eligibility based on study criteria; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; efficiently explains study procedures to address participant/family concerns.
• Routinely ensures timely completion of all study protocol requirements (data entry, data abstraction, and any other related study requirements); evaluates and interprets collected clinical data in conjunction with PI as appropriate; prepares oral or written presentations or reports to the PI as appropriate and provides recommendations or workable solutions for any problems incurring.
• Conducts lab duties, such as blood processing and the shipping of study samples when necessary.
• Performs other duties as assigned by the PI or Senior Clinical Research Coordinator such as additional administrative tasks, literature reviews, grant writing, etc.

Working Conditions:

Job Location/Working Conditions

• Patient care setting.
• On-Call (Beeper)

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:

Clinical Research (2 Years)

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 must be obtained within one month of hire date.
• Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).

Preferred Qualifications

Skills:

Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Database Management, Interpersonal Communication, Organizational Tasks, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)

Grade

C10

Salary Range

$52,600.00 - $78,900.00 / AnnuallyThe salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.