223 Results for

Research Jobs in Fairfield, OH

Jobs

New!

Cincinnati, OH2 days ago

This role requires a seasoned laboratory professional capable of independently performing complex laboratory procedures, supporting clinical study operations, and contributing to specialized workflows critical to Hoxworth's research mission. 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."

New!

Cincinnati, OH2 days ago

Home to 53,235 students, nearly 12,000 faculty and staff and 350,000+ living alumni, UC combines a Top 35 public research university with a physical setting The New York Times has called “the most ambitious campus design program in the country.”. With the launch of Next Lives Here, the Cincinnati Innovation District, a $100 million JobsOhio investment, the oldest and one of the largest cooperative education programs, a dynamic academic health center and entry into the Big 12 Conference, UC’s momentum has never been stronger.

New!

Cincinnati, OH2 days ago

This position joins an active Multidisciplinary Breast Cancer Program within the University of Cincinnati Cancer Center that is triple accreditation from the NAPBC (National Accreditation Program of Breast Centers), NQMBC (National Quality Metrics of Breast Centers), and the ACR (American College of Radiology). 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."

New!

Cincinnati, OH2 days ago

This position joins an active faculty group and busy transplant program dedicated to a clinical practice supporting transplant patients, oncology patients, patients needing vascular access for dialysis or hepatobiliary surgeries; resident teaching activities of surgery residents and fellows; and clinical research. As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients.

New!

Cincinnati, OH2 days ago

Maintain a balanced outpatient and procedural schedule, including: Three (3) half-day outpatient gastroenterology clinics per week; Five (5) half-day endoscopy sessions per week; Establish and lead the first Motility and Neurogastroenterology Clinic at UC, which will involve: Evaluating patients with a full spectrum of neurogastrointestinal and motility disorders, including difficulty swallowing and esophageal motility disorders, abnormal gastrointestinal motility, chronic constipation, functional bowel disorders, disorders of gut–brain interaction, and other complex neurogastrointestinal conditions; Performing comprehensive diagnostic evaluations of complex gastrointestinal motility and related disorders to develop individualized short‑ and long‑term care plans. In addition, many opportunities exist on campus for access to resources in immunobiology, laboratory medicine, transfusion medicine, cell mediated therapy and cancer biology at the University of Cincinnati Medical College, the Hoxworth Blood Center, and the Cincinnati Children’s Hospital Medical Center.

Cincinnati, OH30+ days ago

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." As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients.

Cincinnati, OH17 days ago

This position will provide technical support and assistance under the direct supervision of senior research staff to assist the Principal Investigator and study team on delegated duties to support clinical trials including assistance with the recruitment and retention of research subjects and helping with enrollment screening and consenting. 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."

Cincinnati, OH30+ days ago

As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. Accurately enters data from electronic medical records 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.

Cincinnati, OH30+ days ago

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."

Cincinnati, OH30+ days ago

Remote

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.

Cincinnati, OH30+ days ago

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.

Cincinnati, OH18 days ago

The University of Cincinnati College of Medicine, Department of Internal Medicine, Division of Rheumatology, Allergy and Immunology is seeking either a Research Assistant or Senior Research Assistant to assist with the coordination of laboratory projects or research studies in a particular discipline, make independent contributions to projects and studies based on professional training or functional experience. 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."

New!

Cincinnati, OH4 days ago

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. 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.

Cincinnati, OH30+ days ago

Cincinnati, OH18 days ago

The successful candidate will develop an independent and collaborative research program with external funding potential; contribute to human-subjects imaging research; support MRI protocol development, data acquisition, image analysis, and quality assurance; publish in peer-reviewed journals; participate in grant development; and provide limited mentoring, lecturing, and service as assigned. Areas of particular interest include neuroimaging, artificial intelligence and machine learning for imaging, pulse sequence development, quantitative MRI, image reconstruction, functional MRI, diffusion MRI, perfusion imaging, imaging biomarkers, and translational clinical imaging.

Cincinnati, OH20 days ago

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.

Cincinnati, OH30+ days ago

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.

Kettering, OH30+ days ago

Under the supervision of the Manager, Innovation, Research & Grants at KHN, the CRC I will collaborate with physicians and other healthcare providers, scientists, administration, the Institutional Review Board, Sponsors, and the Food and Drug Administration (FDA). Job Responsibilities: This individual must be able to work independently under limited supervision, while maintaining excellent communication between the principal investigator(s) and all staff involved in any aspect of approved research projects.

Cincinnati, OH30+ days ago

Clinical Research Nurse Sr • Bachelors Degree in Nursing • Current valid RN license to practice in the State of Ohio by date of hire • Two (2) years of clinical nursing experience in a hospital, clinic, or similar healthcare setting • At least two (2) years of clinical trials research experience. • Clinical Research Nurse • Associates Degree • Graduation from an accredited school of nursing • Current valid RN license to practice in the State of Ohio by date of hire • Two (2) years of clinical nursing experience in a hospital, clinic, or similar healthcare setting.

Cincinnati, OH11 days ago

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.

Cincinnati, OH11 days ago

Cincinnati, OH30+ days ago

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.

Cincinnati, OH30+ days ago

Assessment- Assess participants, clients and families, whose needs range from uncomplicated to highly complex and quickly recognize normal parameters, deviations and abnormalities in physical, emotional, developmental and behavioral status based on past nursing experience. Demonstrate critical thinking skills by making appropriate nursing decisions, prioritizing both planned and unplanned events for protocol implementation, and proactively addressing potential and actual problems.

Cincinnati, OH30+ days ago

Remote

Cincinnati, OH30+ days ago

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." UC's 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.

Kettering, OH30+ days ago

Under the supervision of the Manager, Research Finance, provide a full range of administrative duties in support of research finances, research staff and investigators. Job Responsibilities: Proficiency in computer software programs including: Excel, Word, PowerPoint, Access, MS Outlook or similar programs.

Cincinnati, Ohio30+ days ago

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.

Cincinnati, Ohio30+ days ago

Remote

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.

Cincinnati, OH30+ days ago

The position provides excellent hands-on training in cutting-edge cancer biology with direct mentorship from Dr. Czyzyk-Krzeska and close interaction with postdoctoral fellows, graduate students, clinical fellows, and undergraduate researchers. The laboratory investigates the molecular and metabolic mechanisms that drive renal cancer progression using state-of-the-art molecular biology, biochemistry, cell culture, and animal model systems within a highly collaborative and multidisciplinary research environment.

Cincinnati, OH30+ days ago

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 .

Cincinnati, OH30+ days ago

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." Hazards: Includes a variety of physical conditions, such as proximity to moving mechanical parts of machinery or tools used to perform work, moving vehicles, electrical current, working on scaffolding and high places, or exposure to chemicals.

Cincinnati, OH11 days ago

$50,544–$62,150.40 Per Year

Research and improve current methods - Utilize internal and external resources to reproduce, evaluate, research, and improve techniques, bring in new techniques or modify existing techniques. Assists in training post doctoral fellows, graduate students, and junior laboratory personnel in laboratory techniques and equipment.

Springboro, OH15 days ago

This is a unique opportunity for an advanced practice provider in Internal Medicine, Family Medicine, or a related field to contribute to innovative clinical research while maintaining a flexible schedule. ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Dayton, OH research site.

Cincinnati, OH17 days ago

Cincinnati, OH30+ days ago

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.

Cincinnati, OH30+ days ago

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." UC's 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.

Cincinnati, OH18 days ago

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.

Cincinnati, OH30+ days ago

$55,000–$60,000 Per Year

Research Assistant will be responsible for translating system and client needs analysis and development into technical solutions by writing software applications, integrating systems, creating, modifying, and/or supporting desktop, web-based, mobile, cloud, and virtual applications, and application programming interfaces. The SoIT is home to several centers, including an NSADHS Center for Academic Excellence in Cyber Defense, the Information Technology Solutions Center, the Ohio Cyber Range Institute, Applied Machine Learning and Intelligence Center, and the Smart Synergies Lab.

Cincinnati, OH30+ days ago

$56,784–$62,150.40 Per 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.

Cincinnati, OH30+ days ago

Dayton, OH13 days ago

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors'' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.

Cincinnati, OH25 days ago

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.

Cincinnati, OH30+ days ago

The laboratory of Dr. Guo-Chang Fan in the Department of Pharmacology, Physiology, and Neurobiology at the University of Cincinnati College of Medicine is looking for a motivated Research Assistant to assist with the coordination of laboratory projects on macrophage-mediated efferocytosis in cardiovascular disease, maintaining lab animal colonies, and make independent contributions to projects and studies based on professional training or functional experience. 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."

Cincinnati, OH30+ days ago

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; 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. 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 Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

Cincinnati, OH30+ days ago

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. 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 Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

Cincinnati, OH13 days ago

$103,300–$191,900 Per Year

Relationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).

Riverside, OH12 days ago

This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent, educate participants regarding study requirements, event reporting, collection of and organizes research data and complete case report forms. Assists nursing and clinical staff and utilizes knowledge of disease processes to observe, report adverse events, and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.

Cincinnati, OH30+ days ago

In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company. 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.

Cincinnati, OH27 days ago

$50,544–$62,150.40 Per Year

We are seeking a Research Assistant III to contribute to both lab operations and hands-on experimental work, including animal colony management, flow cytometry, and a variety of laboratory assays central to advancing discoveries from bench to bedside. Research and improve current methods - Utilize internal and external resources to reproduce, evaluate, research, and improve techniques, bring in new techniques or modify existing techniques.

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Research Jobs in Fairfield, OH

Sr Research Assistant, Hoxworth Blood Center, Clinical Research University of Cincinnati

Research Nurse Practitioner / Physician Assistant, COM, Department of Psychiatry University of Cincinnati

Assistant / Associate Professor of Surgery, Surgical Oncology University of Cincinnati

Assistant/Associate Professor, Department of Surgery, Division of Transplantation University of Cincinnati

Asst / Assoc / Professor, Department of Internal Medicine, Division of Gastroenterology & Hepatology University of Cincinnati

Clinical Research Assistant, Dean's Office of Clinical Research University of Cincinnati

Clinical Research Assistant, Department of Surgery, Trauma Surgery Research University of Cincinnati

Clinical Research Assistant, Department of Obstetrics and Gynecology University of Cincinnati

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

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

Clinical Research Assistant, UC Cancer Center University of Cincinnati

Research Assistant / Senior Research Assistant, Division of Rheumatology, Allergy & Immunology University of Cincinnati

Research Assistant Gastro Health

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

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

Research Assistant Professor, UC Imaging Research, Development & Innovation Center, Radiology Dept University of Cincinnati

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 Coord I Innovate and Research Kettering Health Network

Clinical Research Nurse / Senior Clinical Research Nurse, UC Cancer Center University of Cincinnati

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 Associate Cincinnati, OH (Entry Level) Medpace Holdings Inc

Research Nurse I/ II, Clinical Research Services Cincinnati Children's Hospital Medical Center

Clinical Research Associate Clinical Research Coordinator Experience Medpace Holdings Inc

Research Instructor / Assistant / Associate / Full Professor, Trauma Surgery Research University of Cincinnati

Clinical Research Assist Innovate and Research Kettering Health Network

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

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

Research Assistant, Czyzyk-Krzeska Lab, College of Medicine, Department of Cancer Biology University of Cincinnati

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

Research Assistant, Division of Hematology & Oncology University of Cincinnati

Research Assistant III - Translational & Clinical Pharmacology - Prasad Lab Cincinnati Children's Hospital Medical Center

Clinical Research Sub-Investigator (NP/PA) ObjectiveHealth Inc

Clinical Research Professional, Department of Neurology & Rehabilitation Medicine, CCBP University of Cincinnati

Clinical Research Nurse Coordinator CTI Clinical Trial Services, Inc.

Clinical Research Professional I or II, Department of Radiology University of Cincinnati

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

Sr. Research Assistant, Information Technology Solutions Center, School of Information Technology University of Cincinnati

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

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

Senior Clinical Research Coordinator Iterative Scopes Inc

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

Research Assistant, Fan Lab, College of Medicine, Dept. of Pharmacology, Physiology, & Neurobiology University of Cincinnati

Clinical Research Associate (Physical Therapist Candidates) Medpace Holdings Inc

Clinical Research Associate (PhD Candidates) Medpace Holdings Inc

Clinical Research Engagement Lead - Northeast Region (Cincinnati, OH) Genentech Inc

Clinical Research Coordinator OhioHealth Corp

Clinical Research Documentation Administrator (TMF) Medpace Holdings Inc

Research Assistant III - Immunobiology - Jordan Lab Cincinnati Children's Hospital Medical Center

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