The Ohio State University
Clinical Research Coordinator
The Ohio State University, Columbus, Ohio, United States, 43224
If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process.
Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following:
Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.
Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.
Clinical Research Coordinator
to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology. Requirements: Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department. This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data. Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols Recruits, interviews and enrolls patients Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements Educates patients and families of purpose, goals, and processes of research study Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements Upkeep of regulatory documents for clinical trials. Collection, processing, transporting of select biological samples for research trials. Other duties as assigned. Preferences: Interest in medical writing including, but not limited to, grant/protocol development and journal articles (reviews and original research) Experience using medical record for clinical data abstraction Experience with database development and management (e.g. RedCap) Prior medical publication history Bachelor’s Degree in biological sciences, health sciences, or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity experience or knowledge in
c linical research required; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Additional Information: Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu . If you have questions while submitting an application, please review these frequently asked questions .
Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.
Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.
Job Title:Clinical Research CoordinatorDepartment:CCC | Comprehensive Cancer Center
Clinical Research Coordinator
to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology. Requirements: Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department.
This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data.
Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
Recruits, interviews and enrolls patients
Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
Educates patients and families of purpose, goals, and processes of research study
Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements
Upkeep of regulatory documents for clinical trials.
Collection, processing, transporting of select biological samples for research trials.
Other duties as assigned.
Preferences: Interest in medical writing including, but not limited to, grant/protocol development and journal articles (reviews and original research)
Experience using medical record for clinical data abstraction
Experience with database development and management (e.g. RedCap)
Prior medical publication history
Minimum Education Requirements: Bachelor’s Degree in biological sciences, health sciences, or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity experience or knowledge in
c linical research required; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Additional Information:
The Ohio State University
is a dynamic community of diverse resources, where opportunity thrives and where individuals transform themselves and the world.
The Ohio State University
is one of the nation’s largest and most comprehensive public universities and a top employer in Ohio. As one of only 57 designated comprehensive cancer centers in the nation,
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital
and
Richard J. Solove Research Institute
is dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies – providing tomorrow’s standard of care today. A Cancer-Free World Begins Here. The OSUCCC – James
is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation’s largest public universities. is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation’s largest public universities. Location:Wiseman Hall (0157)Position Type:RegularScheduled Hours:40 Shift: First Shift
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.
Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions .The university is an equal opportunity employer, including veterans and disability. Create a job alert and receive personalized job recommendations straight to your inbox.
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to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology. Requirements: Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department. This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data. Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols Recruits, interviews and enrolls patients Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements Educates patients and families of purpose, goals, and processes of research study Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements Upkeep of regulatory documents for clinical trials. Collection, processing, transporting of select biological samples for research trials. Other duties as assigned. Preferences: Interest in medical writing including, but not limited to, grant/protocol development and journal articles (reviews and original research) Experience using medical record for clinical data abstraction Experience with database development and management (e.g. RedCap) Prior medical publication history Bachelor’s Degree in biological sciences, health sciences, or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity experience or knowledge in
c linical research required; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Additional Information: Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu . If you have questions while submitting an application, please review these frequently asked questions .
Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.
Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.
Job Title:Clinical Research CoordinatorDepartment:CCC | Comprehensive Cancer Center
Clinical Research Coordinator
to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology. Requirements: Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department.
This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data.
Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
Recruits, interviews and enrolls patients
Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
Educates patients and families of purpose, goals, and processes of research study
Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements
Upkeep of regulatory documents for clinical trials.
Collection, processing, transporting of select biological samples for research trials.
Other duties as assigned.
Preferences: Interest in medical writing including, but not limited to, grant/protocol development and journal articles (reviews and original research)
Experience using medical record for clinical data abstraction
Experience with database development and management (e.g. RedCap)
Prior medical publication history
Minimum Education Requirements: Bachelor’s Degree in biological sciences, health sciences, or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity experience or knowledge in
c linical research required; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Additional Information:
The Ohio State University
is a dynamic community of diverse resources, where opportunity thrives and where individuals transform themselves and the world.
The Ohio State University
is one of the nation’s largest and most comprehensive public universities and a top employer in Ohio. As one of only 57 designated comprehensive cancer centers in the nation,
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital
and
Richard J. Solove Research Institute
is dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies – providing tomorrow’s standard of care today. A Cancer-Free World Begins Here. The OSUCCC – James
is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation’s largest public universities. is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation’s largest public universities. Location:Wiseman Hall (0157)Position Type:RegularScheduled Hours:40 Shift: First Shift
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.
Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions .The university is an equal opportunity employer, including veterans and disability. Create a job alert and receive personalized job recommendations straight to your inbox.
#J-18808-Ljbffr