Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Manages and oversees IRB process for program projects and associated sites, ensuring sites are ...
Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Manages and oversees IRB process for program projects and associated sites, ensuring sites are ...
Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Manages and oversees IRB process for program projects and associated sites, ensuring sites are ...
Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Manages and oversees IRB process for program projects and associated sites, ensuring sites are ...
This position independently coordinates complex regulatory, contractual, financial, and operational ... QUALIFICATIONS 1. Completion of a paralegal or legal studies program or associate's degree in a ...
This position independently coordinates complex regulatory, contractual, financial, and operational ... QUALIFICATIONS 1. Completion of a paralegal or legal studies program or associate's degree in a ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
... IRB's. Job Responsibilities: Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and staff ...
... IRB's. Job Responsibilities: Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and staff ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
... IRB's. Job Responsibilities: * Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and ...
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Project Coordinator*
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Quick apply
Project Coordinator*
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Clinical Research Coordinator
Kettering, OH · On-site
$23.50 - $31.25/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice lt;--- Watch video here ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$23.50 - $31.25/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice lt;--- Watch video here ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$21.50 - $28.75/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice DPN Core Value ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$21.50 - $28.75/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice DPN Core Value ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Project Coordinator* (26.26)
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Project Coordinator* (26.26)
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Project Coordinator* (26.26)
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Project Coordinator* (26.26)
Dayton, OH · On-site
SierTeK proudly serves our clients by providing expertise in the Program Management, Information ... Familiarity with research compliance processes, including IRB, HRPO, IACUC, IBC, or similar ...
Clinical Research Coordinator III - Physical Medicine & Rehabilitation
Cincinnati, OH · On-site
$23.25 - $31/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
Cincinnati, OH · On-site
$23.25 - $31/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
Kettering, OH · On-site
$21.50 - $28.75/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice DPN Core Value ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Kettering, OH · On-site
$21.50 - $28.75/hr
Yearly Bonus Program * Dayton Physicians Network as an Independent Practice DPN Core Value ... IRB requirements. * Essential Duties and Responsibilities: * Coordinates trial activities from ...
Clinical Research Coordinator
Toledo, OH · On-site
$21.75 - $28.75/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$21.75 - $28.75/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$62K/yr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$62K/yr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$21.75 - $28.75/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$21.75 - $28.75/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$22.25 - $29.50/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Clinical Research Coordinator
Toledo, OH · On-site
$22.25 - $29.50/hr
... IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...
Project Coordinator
Dayton, OH · On-site
Aid in managing programs and projects, including drafting project documents, coordinating ... Perform administrative tasks: obtain and maintain applicable IRB, HRPO, IACUC, IBC, and MOU/data ...
Project Coordinator
Dayton, OH · On-site
Aid in managing programs and projects, including drafting project documents, coordinating ... Perform administrative tasks: obtain and maintain applicable IRB, HRPO, IACUC, IBC, and MOU/data ...
Irb Program Coordinator information
What is the difference between Irb Program Coordinator vs IRB Analyst?
| Aspect | Irb Program Coordinator | IRB Analyst |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health, science, or related field; certifications like CITI are common | Similar credentials; often holds certifications such as CITI or IRB-specific training |
| Work Environment | Administrative office, overseeing IRB processes, coordinating meetings, and ensuring compliance | Reviewing protocols, conducting compliance assessments, and supporting IRB decision-making |
| Employer & Industry | Research institutions, hospitals, universities | Research organizations, academic institutions, healthcare facilities |
The Irb Program Coordinator and IRB Analyst roles share similar educational backgrounds and work environments focused on research compliance. The Coordinator manages administrative tasks and communication, while the Analyst focuses more on protocol review and compliance analysis. Both positions are essential in supporting ethical research practices within institutions.
Fetal Center - Clinical Research Program Coordinator
On-site
Nationwide Children's Hospital
• Hospitals • 10K+ employees10,000+ employees
Full-time
Re-posted 18 days ago
Nationwide Children's Hospital rating
7.0
Based on 132 frontline employees who took The Breakroom Quiz
Job description
Overview:
Job Description Summary:
Job Description:
Essential Functions:
- Responsible for administrative management, organization of, and participation in program meetings and teleconferences, including scientific meetings with corporate and non-profit partners, teaching conferences, grand rounds, journal club, research seminars, and CME programs.
- Works with Sponsored Projects Officer to manage program and project funds and dissemination of funding to collaborations sites in addition to the subcontracts with other sites.
- Provides funding opportunity notifications to PI's.
- Collaborates with department/center investigators in the development of IRB protocols, grant submissions and scientific publications.
- Coordinates personnel needs for the program and projects; oversees and organizes training.
- Track projects and initiatives to ensure they move forward based on both timelines and budget; report to PI when progress is lacking and identifies needed action.
- May be responsible for administrative management of multiple protocols; plays a central role in the communication between NCH/RI and site; will act as liaison with other departments necessary to complete program projects (i.e., Data Management, Biostats, Medical Writing, Regulatory Compliance, etc.).
- Manages and oversees IRB process for program projects and associated sites, ensuring sites are submitting accurate and timely IRB submissions, and maintain associated regulatory documents.
- Helps facilitate creation of source documents that ensure systematic data collection and/or aid in protocol execution and management and record keeping.
- Collects and controls research data and subject information from sites as needed/requested; tracks screening and enrollment data across multiple sites/multiple projects.
- Provides monitoring, review and tracking of clinical data and preparation of study specific documents according to FDA regulations QA process implementation, maintenance and documentation; data entry; and maintenance of regulatory documents for multiple sites; multiple protocols.
- Work with principal investigators at each site to establish multi-site monitoring plans for investigator-initiated projects.
Education Requirement:
Bachelor's degree preferred or Associate degree with two years clinical research experience or project management experience.
Certifications:
ACRP or SOCRA certification, preferred.
Skills:
- Demonstrated leadership skills
- Strong organizational skills
- Exceptional interpersonal, written and verbal communication
- Ability to filter information, discern importance and initiate plan for project completion
- Self-directed, results driven with the ability to manage workload.
- Ability to work independently and as part of a team.
- Working knowledge of data management software.
Experience:
Two years clinical research experience or project management experience.
Physical Requirements:
OCCASIONALLY: Bend/twist, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Reaching above shoulder, Squat/kneel
FREQUENTLY: 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