Clinical Research Study Coordinator — Core Center

Cook County Health; Illinois; On-site; USD 62,000 - 70,000; Full time

Benefits offered by this job

Medical, Dental, Vision Coverage

Life Insurance

Pension Plan

Deferred Compensation Program

Paid Holidays, Vacation, and Sick Time

Job summary

Cook County Health is seeking a Research Study Coordinator to manage day-to-day operations of clinical studies at the CORE Center. You will recruit and screen participants, obtain consent, and coordinate study activities under the guidance of the Principal Investigator.

This grant-funded role requires GCP/HSP training, FDA/State guidelines, and experience with medical technology. You will handle data entry, shipping of dangerous goods, and foster timely data submission in a diverse patient

Qualifications

• Bachelor’s degree or higher from an accredited college or university is required (Must provide official transcripts at time of interview).
• One (1) year of experience working in a clinical research or public health setting is required
• Experience preparing shipments of dangerous goods is required
• Experience and knowledge working with medical technology is required
• Must have complete Good Clinical Practice (GCP) training and Human Subjects Protection (HSP) training is required
• Proficiency using Microsoft Office (Excel and Word) is required

Responsibilities

• Coordinates and schedules participant research visits.
• Obtains consent from research participants and ensures participants understand the protocol and what is expected of them while participating.
• Administers interviewer study questionnaires and or interviews.
• Obtains and maintain familiarity and working relationships with an interpreter to support documentation translation services for the purpose of assuring language needs are met for patients contemplating participation in research.
• Completes study protocol procedures according to study specific operating requirements.
• Ensures integrity of data entry, edits, and storage per study protocol.
• Facilitates the collection of medical records per study protocol.
• Coordinates with the research team to facilitate timely data collection and submission.
• Responsible for retention efforts and retaining participants on study, according to the visit schedule set forth by the protocol.
• Prepares shipments of dangerous goods according to relevant guidelines.
• Remains current and updated on relevant State and Federal research guidelines and regulations.
• Performs other duties as assigned.

Skills

Microsoft Office

GCP training

HSP training

Education

Bachelor’s degree or higher

Tools

Excel

Word

Job description

Cook County Health is seeking a Research Study Coordinator to manage day-to-day operations of clinical studies at the CORE Center. You will recruit and screen participants, obtain consent, and coordinate study activities under the guidance of the Principal Investigator.

This grant-funded role requires GCP/HSP training, FDA/State guidelines, and experience with medical technology. You will handle data entry, shipping of dangerous goods, and foster timely data submission in a diverse patient