Top 12 & binders Jobs in Springfield, Il

Clinical Research Regulatory Specialist - SMS-3831
SIU Medicine —Springfield, IL
- $3,657.33 - $4,023.07 a month
- Day shift
- Microsoft Access
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Homeownership Coordinator
The Springfield Housing Authority —Springfield, IL
- $43,578.75 - $65,278.13 a year
- Weekends as needed
- Marketing
- Mid-level
- Driver's License
Quick Apply
Practice Support Associate - South Central Advisor Group
Thrivent —Springfield, IL
- Contract
- Microsoft Excel
- Research
- Administrative experience
Quick Apply
Associate - South Central Advisor Group
Thrivent —Springfield, IL
- Contract
- Research
- Mid-level
- Administrative experience
Quick Apply
Associate - Upper Midwest Advisor Group
Thrivent —Springfield, IL
- Research
- Mid-level
- Administrative experience
Quick Apply
IMMEDIATE HIRE: OTR heavy haul drivers
US Equipment Sales and Rentals —United States
- $100,000 - $150,000 a year
- Urgently hiring
- Clean driving record
- CDL A
- Mid-level
- Fuel card
- Disability insurance
Quick Apply

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Quality Inspector
Cart.com, Inc. —Groveport, OH
Basic math and measurement skills; ability to use measuring tools such as rulers and tape measures. Constant exposure to adverse conditions such as dust, noise,…
Quick Apply
Fulfillment Associate
Cart.com, Inc. —Groveport, OH
Able to lift and carry up to 50 lbs. on occasion (document boxes, files, binders, and other items). Understand and strive to hit your expected target metrics…
Quick Apply
11d

I want to receive the latest job alert for & binders in springfield, il

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

& binders jobs near springfield, il

Support Advisor jobs in Jersey City, NJ

Automotive Service Advisor jobs in Pennsylvania

Support Advisor jobs in Edison, NJ

Help Desk Support Hospital jobs in New York, NY

Non Phone Customer Support jobs in Atlanta, GA

Support Advisor jobs in Colorado Springs, CO

Part Time It Technical Support jobs in Boston, MA

Support Advisor jobs in Oakdale, MN

Retail Tax Office Associate Team Leader jobs in Frankfort, KY

Government Office Cleaning jobs in Washington, DC

Health Science Associate Degree jobs in Atlanta, GA

Retail Tax Office Associate Team Leader jobs in King Of Prussia, PA

Retail Tax Office Associate Team Leader jobs in Portland, OR

Retail Tax Office Associate Team Leader jobs in Raleigh, NC

Otr Drivers jobs in Wisconsin

Otr Trucking jobs in Arkansas

Otr Truck Driver jobs in Sacramento, CA

Otr Team No Experience jobs in Florida

Otr Truck Driver jobs in Orlando, FL

Class B Driver Otr jobs in North Carolina

Clinical Research Regulatory Specialist - SMS-3831

SIU Medicine -
Springfield, IL

Apply Now

Job Details

$3,657.33 - $4,023.07 a month

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Employee assistance program
403(b)
Life insurance
Paid sick time

Qualifications

Computer operation
Bachelor's degree
Desktop applications
Productivity software

Full Job Description

Salary

$3,657.33 - $4,023.07 Monthly

Location

Springfield, IL

Job Type

Principal Administrative

Job Number

2402220

Department

Center for Clinical Research-SMS

Opening Date

07/30/2026

Closing Date

Continuous

FLSA

Non-Exempt

Bargaining Unit

N/A

Shift

Days

Exempt or Non_Exempt

Non-Exempt

SMS/SWS#

SMS-3831

We recommend using the following browsers to complete the application:

Desktop: Google Chrome, Edge with Chromium
Mobile: Google Chrome, Safari

Description

Provide operational support for clinical research and/or research development activities in the Center for Clinical Research (CCR) and participate in research projects for other Departments, as appropriate. This position requires strong interpersonal skills and a basic understanding of the policies and the guidelines that govern clinical research activities.

Examples of Duties

Research: 90%

General

Provides general support to CCR research staff, coordinators, and/or investigators.
Gathers pertinent research documentation (files, medical records, reports, films, etc) and assists research coordinators and investigators to maintaining research data bases, research source documents and case report forms.
May enter patient data into files and automated research databases.
May collect, verify records, and maintain data on clinical activity and/or research; prepares associated reports as required.
May assist in maintaining patient enrollment folders, consent forms, and supplies.
Develops and maintains a positive working relationship within the CCR, outside department, hospital personnel, and outside agencies.
May perform miscellaneous job-related duties as assigned.
Contact research subjects to coordinate and schedule follow-up visits.
Provide follow-up to site monitors, IRB personnel, physicians regarding pertinent patient information when necessary.
May be responsible for on call duties including the use of a beeper.
Attends mandatory CCR and School of medicine-required meetings, and other work-related educational programs.
Gather patients’ related information for studies through hospital records; SIU medical records; physician notes and records.
May perform periodic internal quality assurance audits of study related materials to maintain site readiness for external audits.
May present study information for informed consent and execute informed consent documentation for non-treatment studies.
Clinical
- May perform routine laboratory procedures and patients assessments (i.e., venipuncture).
  Development/Regulatory
- Provides IRB regulatory support to residents and faculty, as directed, including but not limited to preparation of IRB submission materials, development of informed consent documents, maintenance of study approvals.
- Submits protocols and supporting documents to internal and external regulatory
- bodies (i.e., Institutional Review Board), ensuring trials are consistent with
  approved proposals to open new studies.
- Manages and maintains electronic regulatory files (e.g., staff resumes, licenses, training certificates, equipment receipts, investigation logs). Reviews documentation as needed to support regulatory filings, and maintains research files and documentation required by regulations.
- Updates all databases, and regulatory binders with information pertinent to studying
- milestone progress, including but not limited to: IRB databases, internal and external spreadsheets, and study electronic systems.
- Ensures compliance with all applicable local, state, and federal regulations,
- statutes, and laws, and with agencies including the IRB and Federal Drug Administration (FDA). Maintains compliance with Good Clinical Practice (GCP) guidelines, patient confidentiality (HIPAA) and any other applicable laws.
- Maintains communication, attends meetings, and answers questions from all involved parties including regulatory bodies (i.e. IRB), pharmaceutical companies (including monitors), principal investigators and colleagues. Works with clinical trial
  coordinators, research staff and investigators to further communications, helping remove obstacles impeding trial progress.
- May assist with implementation of new regulatory procedures and/or software in accordance with local, state and federal regulations.
- May assist with development of new eREG training materials, protocols, and documentation nomenclatures.
- May assist Regulatory Coordinator in liaison responsibilities between Advarra eREG personnel and CCR eREG development team for best practices for SIU use of eREG.
- May provide assistance to faculty and staff on the use of eREG.
- Assist or performs project-specific literature searches and/or literature reviews as the directed by faculty.
  - May assist in preparing and submission of research abstracts and manuscripts for faculty and resident research projects.
  - May assist faculty with the development of materials necessary for regional and/or national presentation of research results.
  - May assist faculty with basic data analysis needs. Will facilitate statistical support needs for projects using institutional and/or department level statisticians, as directed.
  - May assist faculty with submission of internal or external grant applications.
    
    Teaching: 5%
  - May assist other research staff, residents, and faculty with preparation and presentation of educational content related to clinical research.
  - May instruct other personnel (i.e., technicians, residents, medical students, nurses, investigators) in protocol requirements and/or research methods as needed.
  - May supervise, with support of project faculty mentors, undergraduate interns and medical students participating in clinical research activities.
    Administrative Responsibilities: 5%
  - May order supplies and services required for clinical studies in accordance with the budget and Department/University purchasing guidelines.

Qualifications

Minimum Qualifications:

Graduate of an accredited college with a minimum of a Bachelor’s Degree.
Sensitive to the needs of underrepresented minority populations.

Desired Qualifications:

Must have interpersonal skills necessary to maintain cooperative working relationships with CCR employees, physician faculty, and other research staff.
Must have basic computer skills and be proficient with software packages including, but not limited to, MS Office (Access, Word, Excel, and PowerPoint).
Must have analytical skills necessary in order to gather, organize, and tabulate data.
Knowledge of pharmaceutical and medical terminology.
Should possess a basic understanding of the policies and the guidelines that govern clinical research activities.

Supplemental Information

If you require assistance, please contact the Office of Human Resources at [email protected] or call 217-545-0223 Monday through Friday, 8:00am-4:30pm.

The mission of Southern Illinois University School of Medicine is to optimize the health of the people of central and southern Illinois through education, patient care, research and service to the community.

The SIU School of Medicine Annual Security Report is available online at https://www.siumed.edu/police-security. This report contains policy statements and crime statistics for Southern Illinois University School of Medicine in Springfield, IL. This report is published in compliance with Federal Law titled the
"Jeanne Clery Disclosure of Campus Security Policy and Crime Statistics Act."

Southern Illinois University School of Medicine is an Affirmative Action/Equal Opportunity employer who provides equal employment and educational opportunities for all qualified persons without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, protected veteran status or marital status in accordance with local, state and federal law.

Pre-employment background screenings required.

Apply Now

Refine Your Search

& binders jobs in springfield, il

Clinical Research Regulatory Specialist - SMS-3831

Homeownership Coordinator

Practice Support Associate - South Central Advisor Group

Associate - South Central Advisor Group

Associate - Upper Midwest Advisor Group

IMMEDIATE HIRE: OTR heavy haul drivers

Explore jobs in cities nearby

I want to receive the latest job alert for & binders in springfield, il

Explore jobs in more locations

Description

Examples of Duties

Qualifications

Supplemental Information

Job Seeker Tools

Employer Tools

Browse

Stay Connected