Clinical Research RN - MOB Lindner Research HV - Full Time - Days The Christ Hospital Health NetworkClinical Research RN - MOB Lindner Research HV - Full Time - DaysCincinnati, OHAssists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.
Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days The Christ Hospital Health NetworkClinical Research Nurse-RN - MOB Linder Research HV - Full Time - DaysCincinnati, OHAssists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.
Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days The Christ HospitalClinical Research Nurse-RN - MOB Linder Research HV - Full Time - DaysCincinnati, OHAssists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.
NewClinical Research Coordinator II Velocity Clinical Research, Inc.Clinical Research Coordinator IICincinnati Springdale, OhioTemporaryImplement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
NewClinical Research Manager OHCClinical Research ManagerCincinnati, OhioOHC has served as the region’s premier provider of treatments for cancer and blood disorders, offering a wide range of services and state-of-the-art treatments and technologies, as well as being nationally recognized for cutting edge clinical research breakthroughs in Southwest Ohio area for over 40 years. Collaborates with site research leader (SRL), upper management, and staff in the implementation of action plans designed to improve practice research operations and quality assurance functions.
NewClinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator ICincinnati Springdale, OhioTemporaryCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Clinical Research RN - MOB Lindner Research HV - Full Time - Days The Christ HospitalClinical Research RN - MOB Lindner Research HV - Full Time - DaysCincinnati, OHAssists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.
Dentist, Full Time, First Shift UC HealthDentist, Full Time, First ShiftCincinnati, OHExamines patients, diagnoses dental/oral conditions, prescribes and carries out, or directs others to carry out, appropriate dental/oral treatment, or refers patients for specialty consultation or treatment in conformance with approved clinical protocols and guidelines. UC Medical Center is also home to medical breakthroughs- our physician experts conduct basic, translational and clinical research, leading to new therapies and care protocols, and connecting patients to the latest and most advanced treatments.
Research Associate - I Integrated Resources, IncResearch Associate - ICincinnati, OhioContractorQualificationsEDUCATION / DEGREE / JOB EXPERIENCED REQUIRED: BS or BA preferred, Associate Degree required, preferably in Veterinary Technology, Knowledge of surgical and anesthesia principles, 2 years of veterinary technical experience required (anesthesia experience & surgical support)KEY SKILL / KNOWLEDGE REQUIREMENTS: Knowledge of anatomy and physiology, Ability to work efficiently as a team member, Excellent communication skills – written/oral/listening, Working with limited supervision, as well as comfort with closer guidance, Independent decision making skills as appropriate, Ability to clearly document and communicate plans and results. Research Associate - IA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Cincinnati Clinical Research Project Coordinator Medpace, Inc.Cincinnati Clinical Research Project CoordinatorCincinnati, OhioResponsibilities: Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. 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.
Research Associate-I Integrated Resources, IncResearch Associate-ICincinnati, OhioContractorKnowledge of anatomy and physiology, Ability to work efficiently as a team member, Excellent communication skills – written/oral/listening, Working with limited supervision, as well as comfort with closer guidance, Independent decision making skills as appropriate, Ability to clearly document and communicate plans and results. QualificationsBS or BA preferred, Associate Degree required, preferably in Veterinary Technology, Knowledge of surgical and anesthesia principles, 2 years of veterinary technical experience required (anesthesia experience & surgical support).
Account Analyst Medpace, Inc.Account AnalystCincinnati, OhioIf you are ready to make a difference, you must be able to accomplish these tasks: Responsibilities: Development of fee estimates for requests for proposals (RFPs), budget revisions, and contract amendments; Provides financial input for response to requests for information (RFIs), and ensures coordination of all information with other relevant Medpace personnel as required; Responsible for assuring that bid meets customer’s expectations and specific requirements; Have thorough knowledge of Medpace bid process; Review proposal text assumptions to ensure the fee estimate and proposal text assumptions are consistent; Communicates with Medpace customers regarding ongoing projects to ensure customer’s expectations are being met; Maintain and track ongoing performance of project against budget and notify internal and external clients when potential issues or changes are noted; Review invoices and other financial reports prior to Sponsors receipt; Generate and initiate processing of new contracts and monitor/report on changes in scope, milestone invoicing and/or contract modification to all ongoing contracts in coordination with other employees; Maintain and modify company bid preparation template and boilerplate text to meet changing client needs or specific requirements; May be responsible for other projects and responsibilities as assigned. Qualifications: Bachelor's Degree in Finance, Accounting, or Business; 0-4 years of experience in the conduct of clinical research and/or contract management/pricing; Strong working knowledge of financial and accounting processes; Basic knowledge of medical terminology and a working knowledge of drug development services desired; Excellent analytical, written and oral communication skills; and.
Clinical Trial Project Manager - Infectious Diseases - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Infectious Diseases - CincinnatiCincinnati, OhioResponsibilities: Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Cincinnati, OH office.
Associate Director, Clinical Trial Management Medpace, Inc.Associate Director, Clinical Trial ManagementCincinnati, OhioJob Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group across our US offices. 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 Data Coordinator - Entry Level - Biomedical Engineer Degree Medpace, Inc.Clinical Data Coordinator - Entry Level - Biomedical Engineer DegreeCincinnati, OhioWhen 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. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.
Teaching Assistant, Clinical Nursing Mount Saint Joseph UniversityTeaching Assistant, Clinical NursingCincinnati, OHThe Clinical/Lab Setting: Collaborates with Nursing faculty to evaluate students based on course outcomes; Facilitates integration of theory and research in clinical practice; Makes assignments relevant to course outcomes and students' learning needs: Establishes and maintains a cooperative working relationship with consumers, clinical agencies, and personnel; Communicates goals for students' clinical practice according to specified criteria; Evaluates the clinical agency's effectiveness in providing learning experiences for students. Professional Competencies: Demonstrates knowledge of current trends in healthcare, nursing, and nursing education; Demonstrates creativity in learning strategies, assessment, and nursing practice; Actively participates in professional organizations and community activities; Demonstrates commitment to professional growth; Collaborates with colleagues in nursing and in other disciplines.
Clinical Database Programmer Medpace, Inc.Clinical Database ProgrammerCincinnati, OhioQualifications: Bachelor’s degree in computer science, mathematical science, life science or related field; Basic level experience in at least one programming language; Rave and/or C# or similar programming experience preferred, but not required; Flexible and able to support a variety of studies; Meticulous attention to detail. 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.
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OH Medpace, Inc.Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OHCincinnati, OhioResponsibilities: Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
RN ~ OR Cincinnati Children's Hospital Medical CenterRN ~ ORCincinnati, OH$34–$41.40 / hourExhibits advocacy, moral agency and response to inclusion - Works on behalf of patient and family; assesses personal values; aware of ethical conflicts/issues that may surface in clinical setting; makes ethical/moral decisions based on rules; represents patient when patient cannot represent self; aware of patients' rights. Participates in shared governance at the point-of-care as a member of unit-based councils or by demonstrating awareness and contributing to shared decision making (reading minutes, giving feedback and implementing council decisions).
Clinical Supply Chain Project Specialist (Entry) Medpace, Inc.Clinical Supply Chain Project Specialist (Entry)Cincinnati, OhioPreferred majors: Life Sciences, Supply Chain Management, Operations Management, Business, Math; Minimum 1-year industry experience is preferred; Ability to escalate; Prioritization of daily, weekly, monthly, and project workloads; Strong communication and problem-solving skills; Ability to provide excellent internal and external customer support; Must be flexible and able to work in a risk-based environment and understand multiple potential solutions; Solid working knowledge of Power Point, Excel, Word; and. Responsibilities: As a member of Clinical Packaging and Supplies (CP&S) department you will: Support and collaborate in all activities related to investigational product supply chain, potentially including manufacturing, packaging, labeling, storage, and distribution; Monitor alignment of CP&S timelines with project timelines; Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtual and face to face; and.