277 Results for

Research Coordinator Jobs in Cincinnati, OH

Jobs

Cincinnati, OH

$47,800–$47,800

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The Student Success Coordinator, under the direction of the Director of Student Success, is responsible for administering the scholarship program at the University of Cincinnati Clermont College and providing direct student counseling and support to promote academic success, retention, and graduation.

UC prioritizes work-life balance with a generous time-off policy, including:

Vacation and sick time.

Today

Cincinnati, OH

Remote

p>Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol Communication with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward Verification that the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/drug accountability and inventory Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Must have a minimum of a Bachelor's degree in a health or science related field Experience as a Clinical Research Coordinator (minimum 1 year) Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely Must maintain a valid driver's license and the ability to drive to monitoring sites Proficient knowledge of Microsoft Office Strong communication and presentation skills Must be detail-oriented and efficient in time management.

30+ days ago

Cincinnati, Ohio

Remote

li>SOPs, GCP, and applicable regulatory requirements;

On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;

Verification that the investigator is enrolling only eligible subjects;

Regulatory document review;

Medical device and/or investigational product/drug accountability and inventory;

Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Responsibilities :

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per.

30+ days ago

Cincinnati, OH

This role will entail direct involvement with research participants (children, adolescents, and caregivers), oversight of regulatory compliance, data management support, and leadership within a team of other research coordinators and trainees (e.g., summer and doctoral students, residents, postdoctoral fellows). This position will also include providing strategic support across the Division to promote best practices in research operations, advancing REDCap capabilities, and supporting the successful launch and management of newly funded studies.

26 days ago

Cincinnati, OH

Remote

30+ days ago

Cincinnati, OH

$61,401.60–$78,291.20 / year

Create case report forms (CRFs) in consultation with other team members, as needed, using existing study data information to promote efficient data collection and data entry.

Study Conduct/ Clinical Research Practice - Serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials.

10 days ago

Cincinnati, OH

Full time

Ensure consistency and effective communication during study visits and assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used . Create source templates for study documentation, complete case report forms, and other study specific documents seeking assistance from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed .

30+ days ago

Cincinnati, OH

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, Lindner Center and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

26 days ago

Cincinnati, OH

p>Recruitment, Enrollment, and Retention • Determine best method(s) to identify potential participants for research protocols (advertisements, chart review, monitoring of clinic schedules, etc.) • Create and maintain a detailed tracking system for participants enrolled in study. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

30+ days ago

Cincinnati, OH

Study Conduct/ Clinical Research Practice - Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor. Maintain awareness of study related issues involving investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions.

30+ days ago

Cincinnati, OH

li>Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.

Assists the Principal Investigator and Regulatory Specialist in submission of accurate and timely closeout documents to applicable federal agencies, and the sponsoring agency in accordance with federal regulations and sponsoring agency policies and procedures.

10 days ago

Cincinnati, OH

$56,784–$62,150.40 / year

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.

Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.

30+ days ago

Cincinnati, OH

Full time

Ensure consistency and effective communication during study visits; Assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used. Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed.

30+ days ago

Cincinnati, OH

In this role, the Research Program Coordinator will assist with the planning and implementation of the Research Education & Training programs and will work closely with the Director to coordinate and oversee programs including, but not limited to clinical, education, and community outreach. Implements programs changes to ensure continuity of care as patient or physician needs change.

26 days ago

li>Complete study source documentation; complete/submit case report forms via courier service, fax, or electronic data capture; dispense/collect study drug/device as outlined in the study protocol; maintain study supplies, study drug/device accountability logs, and calibration logs.

Conduct in-services for study staff, review GCP guidelines, maintain GCP &/or CITI certification; obtain/maintain study-specific examiner certification as required by protocol for participating study staff; attend study coordinator meetings.

30+ days ago

Cincinnati, Ohio

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

Responsibilities :

Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Provide oversight and quality control of our internal regulatory filing system;
Manage study supplies;
Create and maintain project timelines; and.
.

30+ days ago

Cincinnati, Ohio

Responsibilities :

Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Provide oversight and quality control of our internal regulatory filing system;
Manage study supplies;
Create and maintain project timelines; and.
.

30+ days ago

Cincinnati, Ohio

Responsibilities :

Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Provide oversight and quality control of our internal regulatory filing system;
Manage study supplies;
Create and maintain project timelines; and.
.

30+ days ago

Cincinnati, OH

$56,784–$62,150.40 / year

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.

5 days ago

Cincinnati, OH

$56,784–$62,150.40 / year

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.

10 days ago

Cincinnati, OH

$56,784–$62,150.40 / year

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.

10 days ago

Cincinnati, OH

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.

3 days ago

Cincinnati, OH

p>• Engage in clinical trial management on a day to day level; • Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; • Compile and maintain project-specific status reports; • Interact with the Sponsor, study sites, and internal associates; • Provide oversight and quality control of our internal regulatory filing system; • Manage study supplies; • Create and maintain project timelines; • Coordinate project meetings and produce quality meeting minutes.

Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

p>• Engage in clinical trial management on a day to day level; • Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; • Compile and maintain project-specific status reports; • Interact with the Sponsor, study sites, and internal associates; • Provide oversight and quality control of our internal regulatory filing system; • Manage study supplies; • Create and maintain project timelines; • Coordinate project meetings and produce quality meeting minutes.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, Ohio

Responsibilities :

Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Provide oversight and quality control of our internal regulatory filing system;
Manage study supplies;
Create and maintain project timelines; and.
.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

Working closely with the principal investigator and research team, the CRC will lead day-to-day study activities, including participant recruitment and scheduling, conducting in-person study visits in Cincinnati, and managing research data.

Study Conduct/ Clinical Research Practice - Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor.

5 days ago

Cincinnati, OH

The Coordinator serves as a key liaison between the Center, faculty, and internal/external stakeholders to streamline the research lifecycle, from initial IRB protocol review to strategic grant scouting and interdisciplinary collaboration. The Center for Research Excellence is seeking a Research and Compliance Coordinator to facilitate Institutional Review Board (IRB) research compliance, proactive grant development, and research training.

24 days ago

Cincinnati, OH

Performs activities in accordance with established policies and procedures related to clinical research study protocols, including but not limited to: answering phone calls, screening participants for eligibility, and registering subjects in Real Time.

10 days ago

Cincinnati, OH

p>This position is responsible for providing administrative and clinical support functions including greeting and scheduling patients, ordering exams, triaging phone calls, filing and maintaining medical records.

REQUIRED SKILLS AND KNOWLEDGE: Photocopier, fax equipment, software and database skills, medical equipment appropriate to research and strong organizational and communication skills.

17 days ago

Cincinnati, OH

This position is responsible for providing administrative and clinical support functions including greeting and scheduling patients, ordering exams, triaging phone calls, filing and maintaining medical records. REQUIRED SKILLS AND KNOWLEDGE: Photocopier, fax equipment, software and database skills, medical equipment appropriate to research and strong organizational and communication skills.

17 days ago

Cincinnati, OH

li>Specific jobs will include assistance with the coordination and delivery of site protocol training for trial specific procedures, collaborate on the development of related educational materials, facilitate scheduling and leading site readiness calls, help with planning investigators' meetings, contribute to the ongoing monitoring of recruitment and retention, and assist with other ongoing internal and external communication of collaborators. Ensuring IRB compliance throughout the study; reviewing site regulatory and staff documents; overseeing the delegation of authority log process; assisting with eConsent management; facilitating IRB approvals for site Principal Investigator changes; tracking and assisting with the clinical trial agreement process, including any modifications throughout the study; and participating in site readiness calls.

24 days ago

Cincinnati, OH

li>Along with data/office-based coordinator(s), accurately enter data from electronic and/or paper research charts into study-specific electronic data capture systems in a timely manner for industry sponsored, federally funded, or investigator initiated clinical research studies.

Under general supervision of the Clinical Research Manager, the Clinical Research Assistant provides support and assistance with clinical trial participants, biospecimens, and data collection to the University of Cincinnati Cancer Center Clinical Trials Office.

13 days ago

Cincinnati, OH

Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting that The New York Times has called the most ambitious campus design program in the country. UCs momentum has never been stronger as the anchor of the Cincinnati Innovation District, the oldest cooperative education co-op program in the country, with students earning $94 million annually through paid experiences, an academic health system, and as a member of the Big 12 Conference.

30+ days ago

Cincinnati, Ohio

Responsibilities :

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;
Verification that the investigator is enrolling only eligible subjects;
Regulatory document review;
Medical device and/or investigational product/drug accountability and inventory;
Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications :
- Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement;
- Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required;
- Must maintain a valid driver’s license and the ability to drive to monitoring sites;
- Proficient knowledge of Microsoft® Office;
- Strong communication and presentation skills; and.

30+ days ago

Cincinnati, OH

p>Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Must have a minimum of a Bachelor's degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver's license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and Must be detail-oriented and efficient in time management.

30+ days ago

Cincinnati, Ohio

17 days ago

Cincinnati, OH

p>The Department of Emergency Medicine, University of Cincinnati College of Medicine is seeking a full-time (100% FTE) Clinical Research Assistant to perform the duties of carrying out our current substance use disorder and harm reduction project as well as other Early Intervention Program grant funded projects. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called "the most ambitious campus design program in the country."

30+ days ago

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Research Coordinator Jobs in Cincinnati, OH

Program Coordinator, Student Success, UC Clermont College University of Cincinnati

Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings Inc

Clinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc.

Clinical Research Coordinator IV or Senior - Behavioral Medicine & Clinical Psychology Cincinnati Children's Hospital Medical Center

Clinical Research Associate Clinical Research Coordinator Experience Medpace Holdings Inc

Clinical Research Coordinator IV - Bone Marrow Transplantation Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator (level dependent on experience) CTI Clinical Trial Services, Inc.

Clinical Research Coordinator II - MOB Lindner Research HV - Full Time - Days The Christ Hospital Health Network

Clinical Research Coordinator II - MOB Lindner Research HV - Full Time - Days The Christ Hospital

Clinical Research Coordinator II/III - Behavioral Medicine & Clinical Psychology - Becker Lab Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator Gastro Health

Clinical Research Coordinator III - Neuromuscular Clinical Trial (Neurology) Cincinnati Children's Hospital Medical Center

Clinical Research Nurse Coordinator CTI Clinical Trial Services, Inc.

Program Coordinator, Research - MOB Lindner Research Admin - Full Time - Days The Christ Hospital

Clinical Research Coordinator - Ophthalmology EyeCare Partners LLC

Clinical Research Coordinator - Ophthalmology Cincinnati Eye Institute

Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic Medpace, Inc.

Clinical Research Project Coordinator - Neuroscience Medpace, Inc.

Cincinnati Clinical Research Project Coordinator Medpace, Inc.

Clinical Research Project Coordinator - Ophthalmology Medpace, Inc.

Clinical Research Project Coordinator - Oncology Medpace, Inc.

Clinical Research Project Coordinator - Infectious Disease Medpace, Inc.

Clinical Research Project Coordinator - Immunology Medpace, Inc.

Clinical Research Project Coordinator - Gastrointestinal/GI Medpace, Inc.

Clinical Research Coordinator III - Hematology Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator III - Mayerson Center Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator III - Bone Marrow Transplantation Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator II/III - Hematology Cincinnati Children's Hospital Medical Center

Clinical Research Project Coordinator Ophthalmology Medpace Holdings Inc

Clinical Research Project Coordinator Neuroscience Medpace Holdings Inc

Cincinnati Clinical Research Project Coordinator Medpace Holdings Inc

Clinical Research Project Coordinator Oncology Medpace Holdings Inc

Clinical Research Project Coordinator Cardiovascular, Renal, Metabolic Medpace Holdings Inc

Clinical Research Project Coordinator Infectious Disease Medpace Holdings Inc

Clinical Research Project Coordinator Gastrointestinal/GI Medpace Holdings Inc

Clinical Research Project Coordinator Immunology Medpace Holdings Inc

Entry-Level Research Project Coordinator Medpace, Inc.

Entry Level Research Project Coordinator Medpace Holdings Inc

Clinical Research Coordinator II/III - Behavioral Medicine & Clinical Psychology Cincinnati Children's Hospital Medical Center

Research & Compliance Coordinator Xavier University

Research Assistant Gastro Health

Clinical Research Administrative Associate - MOB Lindner Research HV - Full Time - Days The Christ Hospital

Clinical Research Administrative Associate - MOB Lindner Research HV - Full Time - Days The Christ Hospital Health Network

Clinical Research Project Manager, Department of Neurology & Rehabilitation, Movement University of Cincinnati

Clinical Research Assistant, UC Cancer Center University of Cincinnati

Clinical Research Professional / Clinical Research Professional II, UC Cancer Center University of Cincinnati

Clinical Research Associate - Cincinnati, OH (Entry-Level) Medpace, Inc.

Clinical Research Associate Cincinnati, OH (Entry Level) Medpace Holdings Inc

Experienced Study Start-Up Coordinator Medpace, Inc.

Clinical Research Assistant, Early Intervention Program, Department of Emergency Medicine University of Cincinnati

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