Research Coordinator-Endo

Nevada System of Higher Education•Skokie, IL

6d•$25 - $37

About The Position

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 Welcome to Endeavor Health Careers At Endeavor Health, we believe every role plays an important part in advancing our mission to help everyone in our communities be their best. Whether you’re just beginning your career journey or are a seasoned professional, you’ll find opportunities here to learn, grow, and thrive. Your Career is our Endeavor. Current Endeavor Health employees: Please do not apply through this site. To be considered, log into Workday and apply using an internal application via the Jobs Hub. For step-by-step instructions, visit ServiceNow and search for the article “Access and View Internal Job Postings.”

Requirements

Bachelor’s degree required, in the fields of social, biological or healthcare sciences preferred
1-5 years of research experience
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

Nice To Haves

Familiarity with clinical data is preferable.
Experience with phlebotomy, ECG and pharmacy practices preferred
CCRP or CCRC; CITI Good Clinical Practice, Human Subjects Research and IATA; 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
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.