Oncology Clinical Data Coordinator

UIC; Chicago, Northern (IL, KY); Hybrid; USD 55,000 - 65,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life Insurance

Retirement Plan

Paid time Off

Tuition waivers for employees and/or a

Job summary

UIC in Chicago, IL is seeking a Clinical Research Data Coordinator for the Cancer Center Clinical Trials Office. You will oversee collection, coordination, processing and quality control of clinical trial data, supporting multiple oncologic studies.

You will collaborate with investigators and staff to ensure protocol adherence, data integrity and regulatory compliance, including specimen handling and study audits. A bachelor’s in science and EMR experience are preferred.

Qualifications

• Bachelor's degree in science or related field is required.
• Minimum of one year of research experience in a healthcare setting.
• IRB and IATA certification preferred or to be completed within 90 days.
• Experience with electronic medical records is a plus.

Responsibilities

• Collaborate with clinical and regulatory coordinators to document and report study patient enrollment, treatment, and follow-up into sponsor’s database.
• Review and synthesize information from medical records to extract trial data per protocol.
• Prepare documents and coordinate the study team for internal and external compliance monitor reviews or audits.
• Handle, process, and ship specimens per study guidelines and safety regulations.
• Manage stock of study kits and other research supplies.
• Perform other related duties and participate in special projects.

Skills

EMR experience

Education

Bachelor degree in science or related field

Tools

Electronic Medical Records (EMR) systems

Job description

UIC in Chicago, IL is seeking a Clinical Research Data Coordinator for the Cancer Center Clinical Trials Office. You will oversee collection, coordination, processing and quality control of clinical trial data, supporting multiple oncologic studies.

You will collaborate with investigators and staff to ensure protocol adherence, data integrity and regulatory compliance, including specimen handling and study audits. A bachelor’s in science and EMR experience are preferred.