Qureos Mentor

The Ohio State University Wexner Medical Center

The Ohio State Wexner Medical Center is a leading healthcare provider in central Ohio, offering a wide range of medical services and conducting significant medical research. With multiple locations throughout the state, it aims to meet all healthcare needs, providing specialized care in areas such as cancer, heart and vascular health, orthopedics, and more. The center is recognized for its commitment to quality patient care and health equity, striving to improve health outcomes in the community.

<div><ul><li>Address:
<div>2255 Kenny Rd</div><div>
Columbus,</div><div>
OH</div>
</li><li>Job Number: R155489
</li><li>Posted Date: 7/30/2026
</li><li>Type: Part time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p>
This position supports a research team by leading manuscript preparation, including conducting literature reviews, synthesizing findings, and drafting first-authored publications for peer-reviewed journals. The role involves qualitative data analysis&mdash;such as reviewing transcripts and applying thematic analysis&mdash;while maintaining rigorous data management practices to ensure accuracy, security, and confidentiality. The Research Associate will also contribute as a co-author on additional lab publications and assist with qualitative data collection involving youth and parents. Compliance with Institutional Review Board (IRB) requirements and ethical research standards is essential. This is an opportunity to produce high-impact scholarship that amplifies diverse voices and informs meaningful change.</p><p></p><p>
Minimum Qualifications:</p><p></p><ul><li>
Doctoral degree or equivalent experience in education, public health, psychology or a related field required.</li><li>
Minimum of 2 years of relevant experience with preparation.</li><li>
Excellent written communication skills with superior attention to detail.</li><li>
Strong creative and analytic thinking abilities with the capacity to generate inferences from analyses.</li></ul><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Research Staff Associate - Psychiatry

<div><ul><li>Address:
<div>7171 Sawmill Pkwy</div><div>
Powell,</div><div>
OH</div>
</li><li>Job Number: R151886
</li><li>Posted Date: 7/30/2026
</li><li>Type: Full time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p>
The Patient Care Associate (PCA) functions as an integral member of a team of care providers on a patient care unit, reflect a</p><p>
culture of cooperation, enthusiasm, and mutual respect. The team, consisting of the Registered Nurse, and the Patient Care</p><p>
Associate provides patient care and supportive services that are directed towards achievement of patient care outcomes,</p><p>
maximizing the patient's involvement in his/her own plan of care, improving services levels, and reducing decreasing</p><p>
costs. Patients and their family will experience the benefits of patient focused care through the integrated skills of all care team</p><p>
members. The Ohio State University Wexner Medical Center is committed to enhancing the quality of care our patients receive.</p><p></p><p>
Minimum Qualifications</p><p>
High School diploma or GED preferred; Previous patient care experience in an acute care hospital setting preferred; Strong customer</p><p>
service, organizational and time management skills; Successful completion of PCA training course required after hire.</p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Patient Care Associate - James Powell Outpatient Clinic

<div><ul><li>Address:
<div>1800 Cannon Dr</div><div>
Columbus,</div><div>
OH</div>
</li><li>Job Number: R156233
</li><li>Posted Date: 7/30/2026
</li><li>Type: Full time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p><b>
SCOPE/SUMMARY</b></p><p>
Clinical Research Assistant providing support to Principal Investigators (PIs) in the Department of Hematology; responsible for reviewing medical records, assisting with patient consent, and assisting with data extraction, tracking patients longitudinally through therapy, date entry and submission. Assisting with data quality control; scheduling and conducting monitoring visits and query resolution; participant screening, recruitment, and bio-specimen collection. Compiles and prepares research data results for manuscripts and presentations. Assists with communication with other disciplines and collaborators to obtain quality data for patients accrued to observational clinical research studies. Follows protocol design to ensure all appropriate data elements are collected in accordance with protocol guidelines. Responsible for internal and external quality assurance and quality reviews. Perform other duties as assigned by PIs and/or supervisor.</p><p></p><p><b>
MINIMUM REQUIRED QUALIFICATIONS</b><br>
Bachelor&rsquo;s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required. 0 years of relevant experience required. 2-4 years of relevant experience preferred.</p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Clinical Research Assistant 2-Hematology

<div><ul><li>Address:
<div>2006-2030 Kenny Rd</div><div>
Columbus,</div><div>
OH</div>
</li><li>Job Number: R155476
</li><li>Posted Date: 7/29/2026
</li><li>Type: Full time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p>
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Department of Neurology/ Division of Cognitive Neurology; 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 clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, &amp; other diagnostic testing in accordance with study protocol; participates in the collection, processing &amp; evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, &amp; provide appropriate level of care; documents unfavorable responses and notifies research sponsors &amp; applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; 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.</p><p></p><p><b>
Minimum Education and Skills/Experience Required/Desired</b></p><p>
Bachelor&rsquo;s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required.</p><p></p><p><b>
Experience Required</b></p><p>
One year experience in a clinical research capacity required.</p><p></p><p><b>
Desired Experience</b></p><p>
2-4 years of relevant experience preferred. Experience or knowledge in cognitive diseases/disorders preferred; knowledge of medical terminology desired; computer skills required with experience using Microsoft Software applications desired.</p><p></p><p><b>
Desired Certification</b></p><p>
Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA).</p><p></p><p><b><i>
Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.</i></b></p><p></p><p><i>
FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research</i></p><p><i>
CAREER BAND: Individual Contributor- Specialized</i></p><p><i>
CAREER LEVEL: S2</i></p>
<p>This is a patient facing position and is required to be onsite.</p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Clinical Research Coordinator 2-Neurology

<div><ul><li>Address:
<div>660 Ackerman Rd</div><div>
Columbus,</div><div>
OH</div>
</li><li>Job Number: R155383
</li><li>Posted Date: 7/20/2026
</li><li>Type: Part time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p></p><p>
The Planning Services Student Assistant is responsible for supporting The Ohio State University Wexner Medical Center&rsquo;s Planning Services Department. The Student Assistant supports facility planners with investigation and analysis of space requests. Support to Interior Design planners, Sr. Planners, Project teams, Environmental Branding, and Signage &amp; Wayfinding includes documenting project work through CAD and Revit drawings and excel spreadsheets. Assistance in areas such as furniture and finish selection extends to all mission areas of the Medical Center space including Clinical, Research, and Academic. Support for signage and graphics includes surveying, concept development, and installation oversight. Global departmental support involves benchmarking research, standards development and documentation.</p><p><b>
Education and Experience
</b></p><p>The Student Assistant is working toward a bachelor&rsquo;s or master&rsquo;s degree in Architecture, Landscape Architecture, Planning, Interior Design, Graphics Design, or similar degree. Completion of at least one semester of course work related to the degree is expected. The person should be dependable and organized, detail oriented, and demonstrate good communication skills (verbal, written, graphic). Must be able to work in 2-4 hour blocks of time and a minimum of 8 hours per week during regular business hours. Work space will be provided at 660 Ackerman Road, with CABS service available from the Medical Center.</p><p></p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Student Assistant - Space and Facilities Planning

<div><ul><li>Address:
<div>3651 Ridge Mill Dr</div><div>
Hilliard,</div><div>
OH</div>
</li><li>Job Number: R154169
</li><li>Posted Date: 7/10/2026
</li><li>Type: Full time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p><b>
Position Summary</b></p><p>
The Clinical Trials Processing Lab handles human fluid and tissue samples from patients enrolled in oncology clinical trials conducted by the James Cancer Hospital.</p><p></p><p>
The Lab Services Lead Coordinator will function independently as the sole technologist at a satellite laboratory location of the CTPL within the Comprehensive Cancer Center.</p><p></p><p><b>
Responsibilities</b></p><ul><li><p>
Helps oversee and manage all activities of the CTPL including preparing labels, labeling tubes for clinical trial specimen collection, specimen processing and storage, retrieving and shipping samples</p></li><li><p>
Uses prescribed laboratory methods, instruments and automated equipment to process clinical patient samples</p></li><li><p>
Prepares necessary supplies for specimen collection</p></li><li><p>
Processes time-sensitive clinical samples for pharmacokinetic, pharmacodynamic and other correlative markers as well as clinical safety labs</p></li><li><p>
Completes laboratory test requisition forms; maintain laboratory maintenance and sample records for audit purposes</p></li><li><p>
Communicates with outside reference labs regarding patient testing, handle inquiries and resolve any testing and/or specimen collection errors</p></li><li><p>
Interacts with clinical research protocol and hospital clinical staff</p></li><li><p>
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical trial specimens, trial and laboratory supplies</p></li><li><p>
Manages sample inventory log and electronic database</p></li><li><p>
Ensures compliance with FDA and IRB regulations as well as internal clinical research SOPs, policies and procedures</p></li><li><p>
Maintains all GCP, IATA, EHS and sponsor-required trainings and certifications</p></li><li><p>
Monitors and ensure periodic and routine maintenance of CTPL equipment</p></li><li><p>
Provides input in developing and revising departmental SOP&rsquo;s</p></li><li><p>
Participates in instruction and training of new clinical laboratory technologists and student assistants</p></li><li><p>
Serves as a CTPL technical expert</p></li><li><p>
Represents the CTPL during sponsor site qualification and monitoring visits</p></li></ul><p></p><p><b>
Job Requirements</b></p><p>
Bachelor&rsquo;s Degree in Biological Sciences, Health related Sciences or equivalent combination of education and experience. 3 years of relevant laboratory experience required.</p>
<p>Clinical Laboratories / Lab Services - Individual Contributor - Specialized - S4 Consultant</p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Lab Services Lead Coordinator, Clinical Trials Processing Lab

<div><ul><li>Address:
<div>460 W 10th Ave</div><div>
Columbus,</div><div>
OH</div>
</li><li>Job Number: R154828
</li><li>Posted Date: 7/10/2026
</li><li>Type: Full time
</li></ul><div><p><b>Current Employees and Students:</b> Please log in to Workday to use the internal job search and application process.</p><p><b>
Position Summary</b></p><div><div><div><div><div><div><div><div><div><p>
Lab Services Coordinator supports all activities of the Clinical Trials Processing Lab by functioning as an integral part of a team in a multi-disciplinary lab and providing services to investigators across the OSUWMC and outside of The Ohio State University.</p><p></p><p><b>
Responsibilities</b></p><ul><li><p>
Assists with all activities of the CTPL including preparing labels and labeling tubes for clinical trial specimen collection, specimen processing, storage, and shipping in compliance with all applicable regulations and institutional policies</p></li><li><p>
Constructs sample libraries of many sample types including, but not limited to, blood, bone marrow, plasma, serum, urine, saliva and paraffin embedded tissue</p></li><li><p>
Assists with data management, inventory control and quality control of human biological specimens</p></li><li><p>
Uses prescribed laboratory methods, instruments and automated equipment; maintain laboratory maintenance records</p></li><li><p>
Prepares necessary supplies for specimen collection</p></li><li><p>
Receives, processes and distributes specimens, including time-sensitive patient samples for pharmacokinetic, pharmacodynamic and other correlative markers as well as safety labs</p></li><li><p>
Manages sample and kit inventory via electronic database</p></li><li><p>
Completes laboratory test requisition forms and maintain samples records for audit purposes</p></li><li><p>
Communicates with outside reference labs regarding patient testing, handle inquiries and resolve any testing and/or specimen collection issues</p></li><li><p>
Interacts with clinical research protocol and hospital clinical staff</p></li><li><p>
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical trial specimens, trial and laboratory supplies</p></li><li><p>
Ensures compliance with FDA and IRB regulations as well as internal clinical research SOPs, policies and procedures</p></li><li><p>
Maintains all GCP, IATA, EHS and sponsor-required trainings and certifications</p></li></ul><p><b><br>
Job Requirements</b></p><p>
Bachelor&rsquo;s Degree in Biological Sciences, Health related Sciences or equivalent combination of education and experience. 1 year of relevant experience required. 2 - 4 years of relevant experience preferred.</p><p></p><p>
Good working knowledge of laboratory principles, equipment and safety standards required; must be able to effectively communicate face to face and in writing with clinical staff and outside collaborators; experience processing tissue, blood, urine, and bone marrow samples, handling bio-hazardous materials and aseptic techniques preferred; data collection and data entry experience required; knowledge of tissue procurement techniques and anatomic pathology desired; knowledge of medical terminology preferred; demonstrates the initiative and ability to provide useful feedback in a professional manner; knowledge of Microsoft Office products including Outlook and Excel required.
</p></div></div></div></div></div></div></div></div></div><p>Clinical Laboratories - Lab Services - Individual Contributor - Specialized - S2 Experienced</p><p>
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.</p><p>
Thank you for your interest in working at Ohio State.</p><p><b><i>
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.</i></b></p><p>
The university is an equal opportunity employer, including veterans and disability.</p></div></div><div></div>

Lab Services Coordinator - Clinical Trials Processing Lab

Join The Ohio State University Wexner Medical Center and explore 15   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.