Clinical Research Coordinator Dayton Physicians NetworkClinical Research CoordinatorKettering, OHDayton Physicians Network is looking to add a Clinical Research Coordinator to our team! Additional accrual increase after 1 year of service with Dayton Physicians!
Clinical Trial Manager Join The CTI TeamClinical Trial ManagerCovington, KentuckyOversight of key clinical monitoring metrics, including but not limited to: Visits scheduled per CTMP, Monitoring Visit Reports (MVR) and associated correspondence timelines, Action Items (AI), query resolution, and other quality metrics, to ensure they are met and followed-up on as necessary. Bachelor's Degree or higher in allied health field such as nursing, pharmacy, or health / natural science, or RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources.
NewClinical Research Coordinator II/III - Bone Marrow Transplantation Cincinnati Children's Hospital Medical CenterClinical Research Coordinator II/III - Bone Marrow TransplantationCincinnati, OHServe 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.
Clinical Research Coordinator III, Various Departments Cincinnati Children's Hospital Medical CenterClinical Research Coordinator III, Various DepartmentsCincinnati, OH$56,784–$62,150.40 / yearCincinnati Children's is seeking talented Clinical Research Coordinators (CRCs) to support innovative clinical and translational research programs across a wide range of specialties, playing a critical role in advancing discoveries that improve child health. CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process research specimens, oversee study data, collaborate with multidisciplinary teams, and ensure compliance with research protocols and regulatory requirements.
Clinical Research Supervisor - Nephrology Cincinnati Children's Hospital Medical CenterClinical Research Supervisor - NephrologyCincinnati, OH$74,297.60–$94,744 / yearWork with faculty, and business director/managers to provide leadership for new project development efforts including development of scope or work, budget and management of contract negotiations, and execution. Strategic Planning - Support the development and implementation of research systems and processes to improve productivity and efficiency and to facilitate sustained growth in collaboration with Principal Investigators.
Clinical Business Intelligence Internship Spring 2027 Medpace Holdings IncClinical Business Intelligence Internship Spring 2027Cincinnati, OHThe Clinical BI Internship position within this team provides a unique opportunity for students who are currently pursuing a business, business technology, computer information systems, or analytics like degree to get hands on experience working across operational functions and a variety of enterprise BI tools, such as Power BI (Visualization tool) and Snowflake (Cloud Database). As an intern on our team, you will contribute across the full development spectrum for new and existing reports - from finding data in our cloud-based data base, manipulating it through SQL, data modeling within Power BI, and creating the report visualizations in Power BI which our end users will interact with.
Clinical Research Coordinator - Ophthalmology Cincinnati Eye InstituteClinical Research Coordinator - OphthalmologyBlue Ash, OHComplete 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 - OphthalmologyBlue Ash, OHComplete 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.
Allergy & Immunology - Clinical Research Faculty Cincinnati Children’s HospitalAllergy & Immunology - Clinical Research FacultyCincinnati, OhioFocus areas of interest are: Anaphylaxis, Chronic Allergic Diseases (lung, respiratory, skin and gastrointestinal tract), Drug Allergy, Eosinophilic Diseases (hypereosinophilia and eosinophilic gastrointestinal disorders), Autoimmunity, Epigenetics, Lymphocyte Biology and Mucosal Immunology, Genetics and Genomics. Cincinnati has all the amenities of a large city including fantastic restaurants, professional sports teams, nationally acclaimed performing arts, ballet, and orchestra with a small-town feel.
Clinical Sales Specialist, Electrophysiology - LAA (Cincinnati/Columbus, OH) AbbottClinical Sales Specialist, Electrophysiology - LAA (Cincinnati/Columbus, OH)Cincinnati, Ohio$68,000–$136,000 / yearIn this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
NewClinical Research Professional, Classical Hematology, Division of Hematology & Oncology University of CincinnatiClinical Research Professional, Classical Hematology, Division of Hematology & OncologyCincinnati, 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.
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."
IDD Clinical Manager ViaQuest IncIDD Clinical ManagerDayton, OHResponsibilities may include: Managing a team of supervisors and mental health case managers including providing guidance and supervision, ensuring comprehensive progress notes are completed for all clients and maintaining ongoing communication regarding client changes and status. Our clients are supported by a team of mental health counselors, social workers, certified nurse practitioners, case managers and psychiatrists to ensure the best outcomes for those we serve.
Clinical Trial Manager BelcanClinical Trial ManagerMason, OHThe CTM role is pivotal for driving robust human testing and clinical trials that are compliant with established governance principles, including ICH-GCP Guidelines. Responsibilities: Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key components of a successful clinical trial.
Clinical Project Coordinator Medpace Holdings IncClinical Project CoordinatorCincinnati, OHProvide day-to-day departmental/project support activities, such as maintenance of project-related files and and IRB document preparation and submissions; Data entry into Medpace proprietary systems and Excel spreadsheets; Coordinate and provide minutes for department/project meetings or conference calls; Maintain spreadsheets and compile reports; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Informatics Intern Spring 2027 Medpace Holdings IncClinical Informatics Intern Spring 2027Cincinnati, OHEnrollment in Bachelor's program for informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to work effectively on a sprint schedule; Strong verbal communication skills; Programming experience in R or Python; Clinical research experience is preferred; Experience building web applications is preferred (with either Shiny or Streamlit); and. Participate in analysts' evaluation of data needs for assigned projects; Work alongside analysts to contribute innovative data products; Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting; Contribute to algorithm development for descriptive, classification, and predictive operational purposes; and.
Clinical Application Support Medpace Holdings IncClinical Application SupportCincinnati, OHInterpret study protocols, protocol amendments, and other relevant operational documents for system set-up; Import data between systems; Act as a liaison between end users and application development teams while maintaining the interests of end users; Develop and implement approaches for the use of software applications as they apply to individual users and study teams; Work with internal and external users to ensure file formats meets systems requirements for to import data files; Write tSQL queries to interact with reporting database when setting up data feeds and integrations, and. Bachelor''s degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field; Good organizational skills, very detail oriented, flexible, and possess good communication skills; Ability to interact with staff and external users from multiple countries; Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project; Demonstrated ability to learn new technologies/applications; Familiar with field's concepts, practices, and procedures; and.
Diagnosis Related Group Clinical Validation Auditor-RN (CDI, MS-DRG, AP-DRG and APR-DRG) Elevance HealthDiagnosis Related Group Clinical Validation Auditor-RN (CDI, MS-DRG, AP-DRG and APR-DRG)Mason, OhioThe Diagnosis Related Group Clinical Validation Auditor-RN is responsible for auditing inpatient medical records to ensure clinical documentation supports the conditions and DRGs billed and reimbursed. Identifies potential documentation and coding errors by recognizing aberrant coding and documentation patterns such aPlease be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health.
Diagnosis Related Group Clinical Validation Auditor-RN(CDI, MS-DRG, AP-DRG and APR-DRG) Elevance HealthDiagnosis Related Group Clinical Validation Auditor-RN(CDI, MS-DRG, AP-DRG and APR-DRG)Mason, OhioThe Diagnosis Related Group Clinical Validation Auditor-RN is responsible for auditing inpatient medical records to ensure clinical documentation supports the conditions and DRGs billed and reimbursed. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
Diagnosis Related Group Clinical Validation Auditor-Rn (Cdi, Ms-Drg, Ap-Drg And Apr-Drg) Elevance HealthDiagnosis Related Group Clinical Validation Auditor-Rn (Cdi, Ms-Drg, Ap-Drg And Apr-Drg)Mason, OH$86,560–$155,808 / yearPreferred Skills, Capabilities and Experiences: One or more of the following certifications are preferred: Registered Health Information Technician (RHIT), Registered Health Information Administrator (RHIA), Certified Clinical Documentation Specialist (CCDS), Certified Documentation Improvement Practitioner (CDIP), Certified Professional Coder (CPC) or Inpatient Coding Credential such as CCS or CIC. Requires a minimum of 10 years of experience in claims auditing, quality assurance, or clinical documentation improvement, and a minimum of 5 years of experience working with ICD-9/10CM, MS-DRG, AP-DRG and APR-DRG; or any combination of education and experience, which would provide an equivalent background.