Acts as a liaison between IRB applicants (faculty, staff, and student investigators), IRB members, and OSPR by corresponding in a timely and professional manner with questions about the IRB process ...
Acts as a liaison between IRB applicants (faculty, staff, and student investigators), IRB members, and OSPR by corresponding in a timely and professional manner with questions about the IRB process ...
Clinical Research Coordinator
$23 - $30.50/hr
Supports IRB submissions and helps prepare manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement ...
Clinical Research Coordinator
$23 - $30.50/hr
Supports IRB submissions and helps prepare manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement ...
Clinical Research Coordinator
$23 - $30.50/hr
Supports IRB submissions and helps prepare manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement ...
Clinical Research Coordinator
$23 - $30.50/hr
Supports IRB submissions and helps prepare manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement ...
Clinical Research Coordinator
Fort Wayne, IN · On-site
$23.85 - $41.96/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file * Comply with reporting of safety related ...
Clinical Research Coordinator
Fort Wayne, IN · On-site
$23.85 - $41.96/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
Indianapolis, IN · On-site
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
Indianapolis, IN · On-site
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
Indianapolis, IN · On-site
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator (RN) - Oncology
Indianapolis, IN · On-site
$24.83 - $46.12/hr
Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file. * Comply with reporting of safety related ...
Clinical Research Coordinator I
$23.75 - $31.50/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
Clinical Research Coordinator I
$23.75 - $31.50/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
Clinical Research Coordinator I
South Bend, IN · On-site
$23.75 - $31.50/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
Clinical Research Coordinator I
South Bend, IN · On-site
$23.75 - $31.50/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
Clinical Research Coordinator I
$19.66 - $34.59/hr
Follows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. Maintains site credentials and ensures updated GCP, licenses ...
Clinical Research Coordinator I
$19.66 - $34.59/hr
Follows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. Maintains site credentials and ensures updated GCP, licenses ...
Clinical Research Coordinator, Pediatric Endocrinology
Indianapolis, IN · On-site
$23.25 - $30.75/hr
This role is responsible for recruiting and screening study participants, coordinating study procedures in compliance with the Institutional Review Board (IRB) and protocol guidelines, and ensuring ...
Clinical Research Coordinator, Pediatric Endocrinology
Indianapolis, IN · On-site
$23.25 - $30.75/hr
This role is responsible for recruiting and screening study participants, coordinating study procedures in compliance with the Institutional Review Board (IRB) and protocol guidelines, and ensuring ...
Clinical Research Coordinator II (3714)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Sponsor-provided and IRB-approved Protocol Training * b. All relevant Protocol Amendments Training * c. Any study-specific Manuals Training, as applicable * d. Sponsor-specified EDC and/or IVRS and ...
Clinical Research Coordinator II (3714)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Sponsor-provided and IRB-approved Protocol Training * b. All relevant Protocol Amendments Training * c. Any study-specific Manuals Training, as applicable * d. Sponsor-specified EDC and/or IVRS and ...
Clinical Trials Operations Consultant (Clinical Research Coordinator)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists with Institutional Review Board (IRB) submissions (initial, continuing review, amendments). * Prepares regulatory binders and essential documents. * Coordinates contract/budget logistics with ...
Clinical Trials Operations Consultant (Clinical Research Coordinator)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists with Institutional Review Board (IRB) submissions (initial, continuing review, amendments). * Prepares regulatory binders and essential documents. * Coordinates contract/budget logistics with ...
Clinical Research Coordinator I
Indianapolis, IN · On-site
$19.66 - $34.59/hr
Follows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. Maintains site credentials and ensures updated GCP, licenses ...
Clinical Research Coordinator I
Indianapolis, IN · On-site
$19.66 - $34.59/hr
Follows Institutional Review Board (IRB) / Independent Ethics Committee (IEC) review, approval and reporting requirements for the site. Maintains site credentials and ensures updated GCP, licenses ...
Clinical Research Coordinator II (3714)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Sponsor-provided and IRB-approved Protocol Training * b. All relevant Protocol Amendments Training * c. Any study-specific Manuals Training, as applicable * d. Sponsor-specified EDC and/or IVRS and ...
Clinical Research Coordinator II (3714)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Sponsor-provided and IRB-approved Protocol Training * b. All relevant Protocol Amendments Training * c. Any study-specific Manuals Training, as applicable * d. Sponsor-specified EDC and/or IVRS and ...
... weekends of call annually * Excellent culture with supportive leadership/mentors who value ... Clinical or basic research opportunities available (40 clinical studies IRB approved, housed within ...
... weekends of call annually * Excellent culture with supportive leadership/mentors who value ... Clinical or basic research opportunities available (40 clinical studies IRB approved, housed within ...
Clinical Research Coordinator
$22.25 - $29.50/hr
Support IRB submissions, amendments, safety reports, and renewals. * Maintain delegation logs and protocol version control. * Promote adherence to SOPs and process improvement initiatives. * Enter ...
Clinical Research Coordinator
$22.25 - $29.50/hr
Support IRB submissions, amendments, safety reports, and renewals. * Maintain delegation logs and protocol version control. * Promote adherence to SOPs and process improvement initiatives. * Enter ...
Pediatric, Nephrology
Indianapolis, IN · On-site
... weekends of call annually * Excellent culture with supportive leadership/mentors who value ... Clinical or basic research opportunities available (40 clinical studies IRB approved, housed within ...
Pediatric, Nephrology
Indianapolis, IN · On-site
... weekends of call annually * Excellent culture with supportive leadership/mentors who value ... Clinical or basic research opportunities available (40 clinical studies IRB approved, housed within ...
Clinical Research Coordinator
$23.25 - $31/hr
Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting. * Maintain research certification on a biannual or triannual basis, as appropriate.
Clinical Research Coordinator
$23.25 - $31/hr
Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting. * Maintain research certification on a biannual or triannual basis, as appropriate.
Weekend Irb information
What is the difference between Weekend IRB vs IRB Coordinator?
| Aspect | Weekend IRB | IRB Coordinator |
|---|---|---|
| Certifications | Often requires IRB-related training, but not always formal certifications | Typically requires IRB or research compliance certifications |
| Work Environment | Part-time, flexible hours, often on weekends or evenings | Full-time, office-based, regular weekday schedule |
| Employer & Industry | Research institutions, hospitals, universities | Research institutions, hospitals, universities |
Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.
What are Weekend IRB jobs?
What are the typical responsibilities of a Weekend IRB member, and how do they contribute to the review process?
What are the key skills and qualifications needed to thrive as an IRB (Institutional Review Board) member, and why are they important?
$16.02/hr
Other
Medical, Dental, Vision, Life, Retirement, PTO
Posted 7 days ago
University Of Southern Indiana rating
7.5
Based on 13 frontline employees who took The Breakroom Quiz
241st of 535 rated colleges and universities
Job description
Apply now Job no: 494254
Work type: Office / Clerical Staff
Location: Evansville
Categories: Office of Sponsored Projects & Research
Title: Research Services Coordinator
Division: Provost's Office
Department: Office of Sponsored Projects & Research
FLSA Status: Non-Exempt
Salary Range: Grade 7: $16.02/hour
EEO Job Group: 5 E5
Position Summary
Provide administration support services for the Office of Sponsored Projects and Research (OSPR), including coordination, administration, and management of human subject research compliance. and support and data maintenance of grant applications
Duties/Responsibilities
Responsible for the day-to-day coordination of IRB (Institutional Review Board) submissions for human subject research and for RCR (Responsible Conduct of Research) committee activities:
Acts as a liaison between IRB applicants (faculty, staff, and student investigators), IRB members, and OSPR by corresponding in a timely and professional manner with questions about the IRB process and modifications required for application approval.
Conducts pre-screening of IRB submissions and communicates with applicants regarding modifications necessary prior to assigning the IRB applications for review by IRB members.
Ensures the timely communication and coordination of necessary documents to enable the IRB members to perform their review tasks.
Creates and distributes modification, approval, disapproval, and continuing review letters to IRB applicants.
Develops competence and maintains compliance with policies and procedures for IRB, RCR, and other research compliance through participation in online webinars and in-person training.
Tracks and coordinates submission review workload of IRB members (e.g., number and types of applications reviewed).
Maintains and updates IRB materials for researchers and IRB members in collaboration with OSPR staff.
Attends IRB and RCR meetings and presentations, takes and maintains meeting minutes, tracks attendance, and prepares end of year letters for IRB members.
Assists with coordination of activities and interactions with the IRB members, other University offices, and IRB investigators.
Serves as a point of contact for Collaborative Institutional Training Initiative (CITI) online training, including verifying training credentials, and maintaining instructions and frequently asked questions (FAQ) documents.
Responsible for regular grant application support and data maintenance:
Maintains, creates and updates grant application information in grant management/administration software (such as Excel).
Creates and distributes internal grant application documents and communications within the University.
Perform tasks related to non-financial pre- and post-award grant administration (such as sending agreements, file progress reports) for both internal and external grants in coordination with OSPR administrative staff.
Develops and maintains competence in policies and procedures for sponsored projects administration through participation in online, webinars, and in-person education.
Conducts data cleaning, analysis of grant applications, prepares data visualizations for regular annual and semester reporting of OSPR grants and Center for Excellence of Teaching and Learning (CETL) faculty development activities.
General office functions:
Creates announcements, such as flyers, and electronic media outreach, to promote OSPR and CETL activities (such as grants opportunities, training events, and workshops).
Gathers and compile information for reports; and other administrative support as necessary to support OSPR and CETL functions.
Receives phone calls and email inquiries for OSPR and determines appropriate action within the office and throughout the University.
Receives, reviews, and distributes incoming mail and email (often confidential); coordinates and schedules meetings; maintains files for OSPR records; copy and distribute documents for OSPR.
Assists with the coordination and conduct of OSPR and CETL events.
Updates and maintains the OSPR website.
Other duties as assigned.
Required Knowledge and Skills
- High school diploma or GED required.
- Three years' related office experience required. A combination of education and experience may be considered.
- Must present a poised, professional first contact for OSPR and be proactive and collaborative.
- Effective and professional oral communication skills and listening skills, and excellent telephone and email etiquette appropriate for interaction with students, faculty, staff, and community members required.
- Effective written communication and proofreading skills, appropriate for creation of correspondence and other documents, required.
- Astute attention to detail and accuracy required.
- Ability to maintain a high level of confidentiality and ethical research standards, and to follow research compliance policies required.
- Effective problem solving while meeting deadlines and the ability to work on multiple projects and tasks with sometimes competing deadlines required.
- Professional interpersonal skills, and effective organization and time management skills required.
- Ability to work with minimal supervision and function as a dependable member of the OSPR team.
- Proficiency in Microsoft Office applications (Word, Excel, Teams, and Outlook) required.
Preferred Knowledge and Skills
- Associate degree, certification(s), or at least two years of college coursework preferred.
- Knowledge of additional Microsoft Office applications and Adobe Acrobat Pro preferred.
- Knowledge of Qualtrics online survey platform preferred.
- Experience with data organization, analysis, and visualization preferred.
- Experience with website maintenance or design preferred.
- Knowledge of the University structure or experience in higher education preferred.
Functional Requirements
- Effective problem solving and the presentation of a professional demeanor while meeting deadlines and achieving critical outcomes, even under demanding conditions such as multiple priorities and short-notice deadlines.
- Ability to use computers and computer systems (hardware and software) to set up functions, enter and organize data, retrieve, process and analyze information, and create documents (such as reports and templates).
- Ability to accurately retrieve and apply information from written documents and from computer-generated reports.
- Positive and professional interactions at all times with staff, faculty, students, and community members, even in difficult situations.
- Remaining in a stationary position at a desk or workstation for extended periods of time for the majority of assigned duties.
- Physical access to other workstations, other departments, and meeting rooms with occasional physical access to events that occur at on-campus sites.
Regular Work Hours/Travel Requirements
- Standard work hours are Monday through Friday, 8:00 a.m. to 4:30 p.m.
- Occasional irregular or overtime hours, including evenings may be required.
- Occasional local travel may be required.
About USI
The University of Southern Indiana is a public higher education institution located on a beautiful 1,400-acre campus in Evansville, IN. We offer employees exceptional benefits! Benefits for this position include:
- Affordable medical, dental, vision, life and short term and long-term disability insurance plans.
- Retirement plan where the University makes the total contribution equivalent to 7% of annual salary.
- Full tuition fee waiver for employees/75% for spouses and dependent children.
- Accrue up to 10 paid vacation days per fiscal year - accrual increases after 4, 7, and 11 years of service
For more information about the benefits that USI offers, please visit www.usi.edu/hr/benefits.
- Cover Letter
- Resume
Pre-Employment Screening
A background check will be required for employment in this position.
Authorization to Work in the United States
USI will not sponsor an employment-related visa for this position.
Interview Accommodations
Persons with disabilities requiring accommodations in the application and interview process please contact the Associate Director of Human Resources, Constance Hermann, at cjhermann1@usi.edu or (812) 461-5363. Contacting the Associate Director of Human Resources is intended for use in seeking disability-related accommodations only. For general applicant inquiries, contact Human Resources at HumanRes@usi.edu or (812) 464-1815.
EEO Statement
USI is an Equal Opportunity Employer as to all protected groups, including protected veterans and individuals with disabilities
Advertised: 02 Jun 2026 Central Daylight Time
Applications close:
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Benefits
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About University of Southern Indiana
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Industry
Colleges, universities, and professional schools
Company size
1,001 - 5,000 Employees
Headquarters location
Evansville, IN, US
Year founded
1965