Registered Dietitian Clinical Research - PRN Professional Case ManagementRegistered Dietitian Clinical Research - PRNCincinnati, OH$42Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career!
Clinical Research Assistant, Department of Surgery, Trauma Surgery Research University of CincinnatiClinical Research Assistant, Department of Surgery, Trauma Surgery ResearchCincinnati, OHThis 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."
Sr Research Assistant, Hoxworth Blood Center, Clinical Research University of CincinnatiSr Research Assistant, Hoxworth Blood Center, Clinical ResearchCincinnati, OHThis 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."
Clinical Research Assistant, Department of Obstetrics and Gynecology University of CincinnatiClinical Research Assistant, Department of Obstetrics and GynecologyCincinnati, OHAs 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.
Clinical Research Assistant, Early Intervention Program, Department of Emergency Medicine University of CincinnatiClinical Research Assistant, Early Intervention Program, Department of Emergency MedicineCincinnati, OHThe 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."
Clinical Research Assistant, UC Cancer Center University of CincinnatiClinical Research Assistant, UC Cancer CenterCincinnati, OHAlong 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.
Research Assistant Gastro HealthResearch AssistantCincinnati, OHCompletes 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.
Clinical Research Professional / Clinical Research Professional II, Department of Psychiatry University of CincinnatiClinical Research Professional / Clinical Research Professional II, Department of PsychiatryCincinnati, OHHome 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.
Clinical Research Professional / Clinical Research Professional II, UC Cancer Center University of CincinnatiClinical Research Professional / Clinical Research Professional II, UC Cancer CenterCincinnati, OHHighlights include: • Salary • Hourly Pay Rate Information • Comprehensive Tuition Remission • Robust Retirement Plans • Work-Life Balance • Additional Benefits Include • Competitive salary based on experience • Comprehensive health coverage, medical, dental, vision, prescription • Flexible spending accounts & wellness programs • Professional development & mentorship opportunities. Job Overview 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 healthcare professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients.
Clinical Research Professional/Clinical Research Professional II, UC Cancer Center University of CincinnatiClinical Research Professional/Clinical Research Professional II, UC Cancer CenterCincinnati, OHHome 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.
Research Assistant Professor, UC Imaging Research, Development & Innovation Center, Radiology Dept University of CincinnatiResearch Assistant Professor, UC Imaging Research, Development & Innovation Center, Radiology DeptCincinnati, OHThe 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.
Clinical Research Nurse / Senior Clinical Research Nurse, UC Cancer Center University of CincinnatiClinical Research Nurse / Senior Clinical Research Nurse, UC Cancer CenterCincinnati, OHClinical 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.
Research Instructor / Assistant / Associate / Full Professor, Trauma Surgery Research University of CincinnatiResearch Instructor / Assistant / Associate / Full Professor, Trauma Surgery ResearchCincinnati, OHHome 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.
Research Nurse I, Clinical Research Services Cincinnati Children's Hospital Medical CenterResearch Nurse I, Clinical Research ServicesCincinnati, OHAssessment- 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.
Clinical Research Associate - Cincinnati, OH (Entry-Level) Medpace, Inc.Clinical Research Associate - Cincinnati, OH (Entry-Level)Cincinnati, OhioResponsibilities: 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.
NewResearch Assistant III/IV - Research Flow Cytometry Facility Cincinnati Children's Hospital Medical CenterResearch Assistant III/IV - Research Flow Cytometry FacilityCincinnati, OHJoin the Research Flow Cytometry Facility at Cincinnati Children's, a centralized shared resource dedicated to providing state-of-the-art flow cytometry instrumentation, cell sorting, training, and technical support to the research community. 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.
NewClinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc.Clinical Research Associate - Clinical Research Coordinator ExperienceCincinnati, OhioRemoteSOPs, 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.
Research Assistant, Timme Lab, College of Medicine, Dept. of Pharmacology, Physiology, Neurobiology University of CincinnatiResearch Assistant, Timme Lab, College of Medicine, Dept. of Pharmacology, Physiology, NeurobiologyCincinnati, OHA full-time Research Assistant position is available in the laboratory of Dr. Nick Timme in the Department of Pharmacology, Physiology, and Neurobiology at the University of Cincinnati College of Medicine to assist with the coordination of laboratory projects or research studies in neuroscience 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."
Clinical Research Coordinator (level dependent on experience) CTI Clinical Trial Services, Inc.Clinical Research Coordinator (level dependent on experience)Cincinnati, OHFull timeEnsure 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 .
Clinical Research Professional I or II, Department of Radiology University of CincinnatiClinical Research Professional I or II, Department of RadiologyCincinnati, OHHome 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.
Clinical Research Coordinator IV - Bone Marrow Transplantation Cincinnati Children's Hospital Medical CenterClinical Research Coordinator IV - Bone Marrow TransplantationCincinnati, OH$61,401.60–$78,291.20 / yearCreate 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.
Clinical Research Nurse Coordinator CTI Clinical Trial Services, Inc.Clinical Research Nurse CoordinatorCincinnati, OHFull timeEnsure 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.
NewResearch Assistant III - Infectious Diseases - Bernstein Lab Cincinnati Children's Hospital Medical CenterResearch Assistant III - Infectious Diseases - Bernstein LabCincinnati, OH$50,544–$62,150.40 / yearJoin the Bernstein Lab at Cincinnati Children's, a nationally recognized research program focused on developing vaccines and treatments for infectious diseases that impact millions worldwide. 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.
Clinical Research Project Manager, Department of Neurology & Rehabilitation, Movement University of CincinnatiClinical Research Project Manager, Department of Neurology & Rehabilitation, MovementCincinnati, OHSpecific 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.
Sr. Research Assistant, Information Technology Solutions Center, School of Information Technology University of CincinnatiSr. Research Assistant, Information Technology Solutions Center, School of Information TechnologyCincinnati, OH$55,000–$60,000 / yearResearch 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.
Clinical Research Coordinator II/III - Hospital Medicine Cincinnati Children's Hospital Medical CenterClinical Research Coordinator II/III - Hospital MedicineCincinnati, OHOur studies focus on topics such as: improving transitions of care from the hospital to home, providing food to hospitalized families who are hungry, reducing monitor overuse, and identifying families in need and connecting them to resources. Rarely, the CRC may help with biospecimen collection, including but not limited to assemble lab kits and/or gather supplies, collect, label, and/or process samples as instructed and deliver or process samples in accordance with the protocol.
Cinical Research Sub-Investigator (NP/PA) ObjectiveHealth IncCinical Research Sub-Investigator (NP/PA)Springboro, OHThis 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.
NewResearch Assistant II/III - Immunobiology - Divanovic Lab Cincinnati Children's Hospital Medical CenterResearch Assistant II/III - Immunobiology - Divanovic LabCincinnati, OHOur group focuses on investigating the development and progression of immune/metabolic/infectious diseases using mouse models and primary human samples through multidisciplinary approaches such as molecular biology, immunology, histopathology, and animal husbandry. 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.
Research Assistant, Fan Lab, College of Medicine, Dept. of Pharmacology, Physiology, & Neurobiology University of CincinnatiResearch Assistant, Fan Lab, College of Medicine, Dept. of Pharmacology, Physiology, & NeurobiologyCincinnati, OHThe 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."
Clinical Research Coordinator II/III - Allergy - Devonshire Lab Cincinnati Children's Hospital Medical CenterClinical Research Coordinator II/III - Allergy - Devonshire LabCincinnati, OHThe Clinical Research Coordinator will play a key role in supporting pediatric clinical research studies, collaborating with patients and families, research teams, and clinical providers to help improve outcomes for children at risk for or living with food allergies. The lab conducts innovative clinical research focused on early-life allergy prevention strategies, food allergy diagnostics, shared decision-making in allergy care, and clinical trials evaluating novel interventions such as oral immunotherapy.
Clinical Research Documentation Administrator (TMF) Medpace Holdings IncClinical Research Documentation Administrator (TMF)Cincinnati, OHIn 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.
Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity Medpace, Inc.Home-Based Experienced CRA (Clinical Research Associate)- Bonus/EquityCincinnati, OhioRemoteResponsibilities: 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: Clinical Research Associate Experience (minimum 1 year); Ability to travel 60-70% to locations nationwide is required; Must have a minimum of a bachelor’s degree in a health or science related field; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.
Clinical Research Coordinator III - (Training & Onboarding Spec) Cancer & Blood Diseases Institute Cincinnati Children's Hospital Medical CenterClinical Research Coordinator III - (Training & Onboarding Spec) Cancer & Blood Diseases InstituteCincinnati, OH$56,784–$62,150.40 / yearThe role serves as a highly visible representative of the clinical research division and works collaboratively with research staff, faculty, sponsors, contract research organizations (CROs), and institutional partners to foster a supportive, efficient, and compliant research environment. This position oversees protocol training and onboarding activities for Oncology, Hematology, and Bone Marrow Transplantation research personnel while supporting division-wide operational initiatives, process improvement efforts, and special projects.
Research Assistant III/IV - Single Cell Genomics Facility Cincinnati Children's Hospital Medical CenterResearch Assistant III/IV - Single Cell Genomics FacilityCincinnati, OH$52,624–$62,150.40 / yearEffectively communicate with team members and contribute to their growth by sharing knowledge, experience, and skills; stay abreast of changes in key systems; serve as an expert resource to the department, and/or hospital in specific area(s). We are seeking a Research Assistant III or IV to support microbial metagenomics projects involving both wet-lab molecular biology techniques and data analysis.
Research Assistant, Biological Sciences, College of Arts and Sciences University of CincinnatiResearch Assistant, Biological Sciences, College of Arts and SciencesCincinnati, OHHazards: 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. 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."
Research Assistant II/III/IV - Infectious Diseases - Way Lab Cincinnati Children's Hospital Medical CenterResearch Assistant II/III/IV - Infectious Diseases - Way LabCincinnati, OH$20.57–$25.72 / hourEffectively communicate with team members and contribute to their growth by sharing knowledge, experience, and skills; stay abreast of changes in key systems; serve as an expert resource to the department, and/or hospital in specific area(s). As a Research Assistant in the Way Lab at Cincinnati Children's, you will support innovative immunological research aimed at improving pregnancy outcomes and enhancing newborn immunity.
Human Genetics - Assistant or Associate Professor- Research - Tenure Cincinnati Children's Hospital Medical CenterHuman Genetics - Assistant or Associate Professor- Research - TenureCincinnati, OHLead program development for service and/or administration as evidenced by contributions including: leadership role in the development of innovative programs for research and/or patient care of educational purposes; significant leadership role in the direction of an academic division; leadership role in the medical center or university; leadership role in regional & national professional societies, program committees and governing boards. The institution is the third‑highest NIH-funded pediatric hospital and supports discovery through 1.4 million square feet of research space and extensive core facilities, including high‑throughput DNA analysis, biomedical informatics, genome editing, pluripotent stem cell resources, animal and viral vector facilities, mass spectrometry, biobanking, and the Applied Gene and Cell Therapy Center.
Clinical Research Coordinator - Ophthalmology Cincinnati Eye InstituteClinical Research Coordinator - OphthalmologyOHComplete 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.
Clinical Research Coordinator - Ophthalmology EyeCare Partners LLCClinical Research Coordinator - OphthalmologyOHComplete 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.
Clinical Research QA Specialist - Pulmonary Cincinnati Children's Hospital Medical CenterClinical Research QA Specialist - PulmonaryCincinnati, OH$56,846.40–$72,488 / yearPrepare and execute monitoring plans both internally and at affiliate sites, including site visits to ensure protocol and regulatory compliance; data management tasks to ensure study data integrity; verify essential documents are accurate, complete, and maintained; and coordination of applicable follow-up activities. Monitoring - Develop comprehensive data safety monitoring plans for all clinical trial activities within the assigned department to ensure that trials are conducted in compliance with the protocol, SOPs, ICH GCP, federal, state, and local regulatory requirements.
Clinical Research Project Coordinator Immunology Medpace Holdings IncClinical Research Project Coordinator ImmunologyCincinnati, OHEngage 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.
Clinical Research Project Coordinator Neuroscience Medpace Holdings IncClinical Research Project Coordinator NeuroscienceCincinnati, OHEngage 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.
Clinical Research Project Coordinator Ophthalmology Medpace Holdings IncClinical Research Project Coordinator OphthalmologyCincinnati, OHEngage 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.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Covington, KentuckyRemoteFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Documentation Administrator (TMF) Medpace, Inc.Clinical Research Documentation Administrator (TMF)Cincinnati, OhioManage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and. 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.
Biomedical Informatics - Assistant Professor, Associate Professor, Research Cincinnati Children's Hospital Medical CenterBiomedical Informatics - Assistant Professor, Associate Professor, ResearchCincinnati, OHService and/or Administration: - Participates in program development for service and/or administration as evidenced by one of the following: make contributes to the development of a research or educational programs or take a role in the direction of a research area or division; or provide consultation on a specific program development; or participates in performance improvement programs or on divisional, departmental, or research committees (i.e., IRB); participates in local or regional research/scientific affairs through membership in societies or specialty governing boards. Demonstrate advancing contributions to research and teaching including: recognition as a teacher, role model and mentor internally; may lead research, teaching, training program; outside recognition of research or teaching as demonstrated by local and/or regional; contributes toward the development and direction of research and/or educational program at the division, department or system level.
Clinical Research Coordinator Dayton Center for Neurological DisordersClinical Research CoordinatorCenterville, OhioKey Responsibilities of a Clinical Research Coordinator include but are not limited to: Participant Recruitment and Management: Identifying, screening, and enrolling eligible participants, obtaining informed consent, and managing participant data. Knowledge of Regulatory Guidelines: Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements Experience Requirement: Experience as a Coordinator in a medical office Research Department (required) .
Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.Experienced Clinical Research Associate - Hematology/OncologyCincinnati, OhioCandidates must have at minimum a Bachelor’s degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills. 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.
Clinical Research Project Coordinator - Infectious Disease Medpace, Inc.Clinical Research Project Coordinator - Infectious DiseaseCincinnati, OhioResponsibilities: 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.
Clinical Research Project Coordinator - Gastrointestinal/GI Medpace, Inc.Clinical Research Project Coordinator - Gastrointestinal/GICincinnati, OhioResponsibilities: 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.