Research Coordinator-Endo
NorthShore University HealthSystem, Skokie, IL, United States
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
#J-18808-Ljbffr
$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
#J-18808-Ljbffr