Clinical Research Coordinator I (Part Time) - Pediatrics Adolescent Medicine

Clinical Research Coordinator

Assists Principal Investigator (PI) as coordinator of a basic to moderately 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 ensuring regulatory compliance.

Primary Duties & Responsibilities:

• IRB support
• Assist the PI in drafting study protocols; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with project participants, research administration staff, and funding or sponsoring agency.
• Financial oversight
• Assists the PI and pre-award team with drafting project budgets and budget justifications
• Supports the PI in oversight of budget utilization for each research project
• Orders gifts cards for study participants; orders meal for project events; arranges transportation for project participants; submits receipts for reimbursement, including participant compensation; maintains necessary tax records
• Project infrastructure and data management
• Assists with compliance related to assent/consent procedures
• Manages research team meeting schedules; schedules meetings with community partners, participant interviews/focus groups/group sessions; reserves rooms for group meetings; sends reminders to participants before meeting dates
• Coordinates copying, printing, and mailing of study-related materials
• Ensures availability of materials (e.g., nametags, flipcharts, writing instruments) for research team meetings and study sessions
• Creates surveys in REDCap; distributes surveys to participants and tracks completion; generate data quality checks; provides quarterly data summaries; maintains data dictionaries, codebooks, and other study metadata
• Drafts facilities, resources, and related documents for grant submissions
• 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:

• 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:

Clinical (2 Years), Administrative (2 Years)

Skills: Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Interpersonal Communication, Organizing, Research Support

Salary Range: $22.78 - $34.21 / Hourly

All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.