Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) andof Investigational New Drug Applications (IND's) to the U.S. Food and Drug Administration (FDA)
Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) andof Investigational New Drug Applications (IND's) to the U.S. Food and Drug Administration (FDA)
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
Clinical Research Coordinator
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
Clinical Research Coordinator
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
Clinical Research Coordinator
Cincinnati, OH · On-site
$23.25 - $31/hr
Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...
... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ... Ensure compliance with IRB/FDA standards and deadlines in the following: notification of subject ...
... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ... Ensure compliance with IRB/FDA standards and deadlines in the following: notification of subject ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
... IRB/FDA compliance, supporting subject enrollment, and trial oversight. This role is ideal for ... No Weekend, Holiday or On Call Commitment Benefits: TriHealth offers a comprehensive benefits ...
Clinical Research Coordinator
Dayton, OH · On-site
$25 - $35/hr
This is an outstanding opportunity to join a full-time (M-F, no holidays or weekends!) outpatient ... Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements Key ...
Clinical Research Coordinator
Dayton, OH · On-site
$25 - $35/hr
This is an outstanding opportunity to join a full-time (M-F, no holidays or weekends!) outpatient ... Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements Key ...
Clinical Research Coordinator
Kettering, OH · On-site
$23.50 - $31.25/hr
Monday through Friday 8:00am - 4:30pm No weekends, evenings or holidays! Work/life balance ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$23.50 - $31.25/hr
Monday through Friday 8:00am - 4:30pm No weekends, evenings or holidays! Work/life balance ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$21.50 - $28.75/hr
Monday through Friday 8:00am - 4:30pm No weekends, evenings or holidays! Work/life balance ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$21.50 - $28.75/hr
Monday through Friday 8:00am - 4:30pm No weekends, evenings or holidays! Work/life balance ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator-Hematology
$23.50 - $31.25/hr
Assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC ...
Clinical Research Coordinator-Hematology
$23.50 - $31.25/hr
Assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC ...
Clinical Research Coordinator-Hematology
Columbus, OH · On-site
$22 - $29.25/hr
Assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC ...
Clinical Research Coordinator-Hematology
Columbus, OH · On-site
$22 - $29.25/hr
Assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC ...
$23.75 - $31.50/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
$23.75 - $31.50/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
$23.75 - $31.50/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
$23.75 - $31.50/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
Clinical Research Coordinator III - Physical Medicine & Rehabilitation
$23.02 - $33.09/hr
Tasks include completing project/IRB regulatory tasks, program/content development, scheduling and coordinating trainings and planning meetings, contacting/enrolling participants, data collection ...
Clinical Research Coordinator III - Physical Medicine & Rehabilitation
$23.02 - $33.09/hr
Tasks include completing project/IRB regulatory tasks, program/content development, scheduling and coordinating trainings and planning meetings, contacting/enrolling participants, data collection ...
Clinical Research Coordinator Social & Behavioral Sciences I
Columbus, OH · On-site
$23.50 - $31.25/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
Clinical Research Coordinator Social & Behavioral Sciences I
Columbus, OH · On-site
$23.50 - $31.25/hr
Recruits, consents, and enrolls according to regulations and subjects' rights through institutional IRB, federal, and state regulations, while adhering to quality control guidelines and institutional ...
Clinical Research-RN - MOB Lindner Research HV - Full Time - Days
Cincinnati, OH · On-site
$66K - $83K/yr
Submits serious adverse events (SAEs) to the IRB and sponsor per established guidelines ... one weekend every three months. * Assists in training of new staff as needed. * Demonstrates ...
Clinical Research-RN - MOB Lindner Research HV - Full Time - Days
Cincinnati, OH · On-site
$66K - $83K/yr
Submits serious adverse events (SAEs) to the IRB and sponsor per established guidelines ... one weekend every three months. * Assists in training of new staff as needed. * Demonstrates ...
Clinical Research RN - MOB Lindner Research HV - Full Time - Days
Cincinnati, OH · On-site
$66K - $83K/yr
Submits serious adverse events (SAEs) to the IRB and sponsor per established guidelines ... one weekend every three months. * Assists in training of new staff as needed. * Demonstrates ...
Clinical Research RN - MOB Lindner Research HV - Full Time - Days
Cincinnati, OH · On-site
$66K - $83K/yr
Submits serious adverse events (SAEs) to the IRB and sponsor per established guidelines ... one weekend every three months. * Assists in training of new staff as needed. * Demonstrates ...
Clinical Research Coordinator I
Akron, OH · On-site
$23.25 - $30.75/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
Akron, OH · On-site
$23.25 - $30.75/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 ...
Weekend Irb information
What is a weekend IRB?
Weekend IRB jobs refer to positions related to Institutional Review Boards (IRBs) that operate or require work during weekends. IRBs are committees established to review and approve research involving human subjects, ensuring ethical standards are met. Weekend IRB staff may include coordinators, administrators, or reviewers who process submissions, review protocols, and ensure compliance outside of normal weekday hours to accommodate researchers' needs and deadlines.
What are the typical responsibilities of a weekend IRB member?
As a Weekend IRB (Institutional Review Board) member, your primary responsibility is to review research protocols submitted for ethical and regulatory compliance, particularly those requiring urgent or expedited consideration over weekends. This role often involves collaborating remotely with fellow board members, principal investigators, and compliance staff to ensure timely feedback on submissions. Challenges may include balancing multiple protocols with tight deadlines and maintaining clear communication despite limited in-person interaction. Your input directly impacts participant safety and institutional compliance, making attention to detail and ethical judgment essential.
What are the key skills and qualifications needed to thrive as a weekend IRB member?
To thrive as an IRB member, you generally need a background in research ethics, regulatory compliance, and relevant academic or clinical experience, often supported by advanced degrees in health, law, or social sciences. Familiarity with federal regulations (such as 45 CFR 46), online protocol management systems, and human subjects protection certifications (e.g., CITI Program) is typically required. Strong analytical thinking, attention to detail, impartiality, and effective communication skills distinguish outstanding IRB members. These skills ensure that research protocols are ethically reviewed, participant rights are protected, and institutional compliance is maintained.
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.
How to get a Weekend IRB job?
To get a Weekend IRB job, candidates should have relevant experience in research or clinical settings, often requiring knowledge of regulatory compliance and ethical review processes. Strong organizational skills and the ability to work independently during weekends are important. Applying through job boards, networking within research institutions, and obtaining certifications like GCP can improve chances.
What are the most commonly searched types of Irb jobs in Ohio?
The most popular types of Irb jobs in Ohio are:
Senior Research Regulatory Coordinator - RI Gene Ther
Columbus, OH • On-site
Full-time
Posted 15 days ago
Nationwide Children's Hospital rating
6.9
Based on 131 frontline employees who took The Breakroom Quiz
549th of 1,061 rated hospitals
Job description
Overview:
Job Description Summary:
Coordinates the regulatory and compliance process of all clinical research conducted in the NCH/RI system. Oversees the preparation and submission of regulatory and compliance documents to study sponsors and assists with quality improvement initiatives. Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) andof Investigational New Drug Applications (IND's) to the U.S. Food and Drug Administration (FDA).
Job Description:
Essential Functions:
Education Requirement:
Bachelor's degree or equivalent experience in medical/science field.
Licensure Requirement:
(not specified)
Certifications:
CCRP certification preferred.
Skills:
Knowledge of medical terminology and diseases, preferred.
Excellent computer skills.
Ability to multi-task with strong organizational and prioritization skills.
Strong attention to detail.
Customer focused personality.
Working knowledge of IRB and regulatory processes and systems.
Current knowledge of Federal regulations (FDA, GCP, NIH, DHHS, ICH GCP), and study protocols.
Experience:
Two years Clinical Research Experience, required.
Physical Requirements:
OCCASIONALLY: Bend/twist, Driving motor vehicles (work required) *additional testing may be required, Reaching above shoulder, Squat/kneel
FREQUENTLY: Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Sitting, Standing, Walking
CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near
Additional Physical Requirements performed but not listed above:
(not specified)
"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"
Job Description Summary:
Coordinates the regulatory and compliance process of all clinical research conducted in the NCH/RI system. Oversees the preparation and submission of regulatory and compliance documents to study sponsors and assists with quality improvement initiatives. Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) andof Investigational New Drug Applications (IND's) to the U.S. Food and Drug Administration (FDA).
Job Description:
Essential Functions:
- Reviews study protocols in order to write consent/assent documents and develop the initial IRB submission; submits protocol amendments; responds to contingencies and obtains final approval of documents from sponsor and IRB, on behalf of principal investigator.
- Serves as liaison between study sponsors and the research team (IRB, research staff and Principal Investigator) regarding regulatory matters in the IRB submission and approval process.
- Responsible for the preparation, submission and maintenance of documents and processes related to investigator-initiated drug/device projects. Serves as liaison with federal agencies as needed.
- Oversees the creation and maintenance of regulatory documents and the study administrative binder required for the clinical research project.
- Maintains current knowledge of federal research regulations by reviewing current publications and attending conferences. Advises management of regulation changes and projected impact within Clinical Research Services and the institution.
- Primary resource to provide guidance to investigators and research staff on federal regulations, good clinical practices and IRB policies and systems. Identifies protocol content which may conflict with federal and/or local requirements or practice.
- Assists with quality improvement audits, including the administrative binder, subject research records, case report forms and other study documents.
- Responsible for data required for CCTS annual report and other metrics as required.
Education Requirement:
Bachelor's degree or equivalent experience in medical/science field.
Licensure Requirement:
(not specified)
Certifications:
CCRP certification preferred.
Skills:
Knowledge of medical terminology and diseases, preferred.
Excellent computer skills.
Ability to multi-task with strong organizational and prioritization skills.
Strong attention to detail.
Customer focused personality.
Working knowledge of IRB and regulatory processes and systems.
Current knowledge of Federal regulations (FDA, GCP, NIH, DHHS, ICH GCP), and study protocols.
Experience:
Two years Clinical Research Experience, required.
Physical Requirements:
OCCASIONALLY: Bend/twist, Driving motor vehicles (work required) *additional testing may be required, Reaching above shoulder, Squat/kneel
FREQUENTLY: Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Sitting, Standing, Walking
CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near
Additional Physical Requirements performed but not listed above:
(not specified)
"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"
What Nationwide Children's Hospital employees say
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About Nationwide Children's Hospital
Sourced by ZipRecruiter
Nationwide Children's Hospital, established in 1894, is a leading pediatric healthcare system based in Columbus, Ohio, United States. They serve as a primary pediatric network, providing wellness, preventive, diagnostic, treatment, and rehabilitative care for infants, children, adolescents, and adults with congenital disease. Being the third-largest pediatric hospital in the nation, Nationwide Children's Hospital prides itself on its relentless commitment to children and their families, driven by their core values of respect, integrity, determination, empathy, and solidarity. The institution's comprehensive mission is to enhance the health of children by providing high-quality, family-centered care, conducting groundbreaking research, advocating for pediatric health, and training top healthcare professionals.
Industry
Hospitals
Company size
10,000+ Employees
Headquarters location
Columbus, OH, US
Year founded
1892