Research Coordinator-Infectious Disease

Endeavor Health•Skokie, IL

1d•Hybrid

About The Position

Provides clinical care services including consenting, treating and monitoring of patients. Recruit and screen candidates for clinical trials. Acquire past medical and medication history profiles. Ship lab samples. Dispense research drug to patients according to protocol. Utilize electronic capture to update patient information. Helps to oversee clinical data for audits and oversight visits. Perform a variety of research, data entry and regulatory duties of a routine and technical nature related to departmental research endeavors. Ensure adherence to protocols and quality of information received. Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol. Assist with budget proposals and study budget tracking. Assist with study time reporting. Ensure compliance with local, state and Federal regulations for the protection of human subjects. Complete regulatory submissions/revisions for the Institutional Review Board (IRB). Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion. Complete data abstraction and data entry for study specific databases. Review and timely report study related adverse events to the sponsor.

Requirements

High School diploma required
1-5 years of research experience

Nice To Haves

Bachelor’s degree preferred, in the fields of social, biological or healthcare sciences preferred
Experience with phlebotomy, ECG and pharmacy practices preferred

Responsibilities

Provides clinical care services including consenting, treating and monitoring of patients
Recruit and screen candidates for clinical trials
Acquire past medical and medication history profiles
Ship lab samples
Dispense research drug to patients according to protocol
Utilize electronic capture to update patient information
Helps to oversee clinical data for audits and oversight visits
Perform a variety of research, data entry and regulatory duties of a routine and technical nature related to departmental research endeavors
Ensure adherence to protocols and quality of information received
Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol
Assist with budget proposals and study budget tracking
Assist with study time reporting
Ensure compliance with local, state and Federal regulations for the protection of human subjects
Complete regulatory submissions/revisions for the Institutional Review Board (IRB)
Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion
Complete data abstraction and data entry for study specific databases
Review and timely report study related adverse events to the sponsor