Research Coordinator-Endo

Hourly Pay Range:

$24.86 - $37.29 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors.

Position Highlights

• Position: Research Coordinator-Endo
• Location: Skokie, IL & locations to other sites will be required
• Full Time/Part Time: Full Time
• Hours: Monday-Friday
• Required Travel: possible travel to study start-up meetings

What you will do:

• Excellent interpersonal skills and the ability to interact in a professional and sensitive manner handling financial information, research project information, research proposals, IRB paperwork.
• Excellent organizational skills and attention to detail
• Computer literacy in Microsoft Word, Excel, Power Point
• Familiarity with clinical data is preferable.
• 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
• Obtain, process and ship biological lab samples
• Dispense research drug to patients according to protocol.
• Utilize electronic capture to submit and update patient information.
• Prepare for routine audits and oversight visits
• Perform a variety of research, data entry and regulatory duties of a routine and technical nature within the required time frames
• 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 developing study budget proposals and tracking study expenditures
• 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.

What you will need:

• Education: Bachelor’s degree required, in the fields of social, biological or healthcare sciences preferred
• Experience: 1-5 years of research experience
• Skills: Experience with phlebotomy, ECG and pharmacy practices preferred
• Certifications/Trainings: CCRP or CCRC; CITI Good Clinical Practice, Human Subjects Research and IATA; preferred

Benefits:

• Career Pathways to Promote Professional Growth and Development
• Various Medical, Dental, and Vision options
• Tuition Reimbursement
• Free Parking at designated locations
• Wellness Program Savings Plan
• Health Savings Account Options
• Retirement Options with Company Match
• Paid Time Off and Holiday Pay
• Community Involvement Opportunities