Clinical 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 Nurse TriHealth IncClinical Research NurseCincinnati, OHActs as a liaison between Study Sponsors, Study Monitors, Principal Investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a clinical research study. Actively participate in the selection of studies TriHealth conducts, developing a process for implementation of the protocol, participating in the identification of potential subjects, participating in the informed consent process, enrolling subjects and accurately and thoroughly collecting and reporting data.
Senior Clinical Research Associate IRESenior Clinical Research AssociateCincinnati, Ohio$110,520–$138,150 / yearWilling and able to travel up to 50% for on-site monitoring visits across northeast region; preference given to candidates residing in Cincinnati, OH near major HUB airports to support efficient regional travel. Senior Clinical Research Associate- Oncology- Ohio ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II Allen SpoldenClinical Research Associate IICleveland, OhioConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Thermo Fisher Scientific IncExperienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas AvailableOH$66,800–$125,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Clinical Research Site Relationship Coordinator Medpace Holdings IncClinical Research Site Relationship CoordinatorCincinnati, OHThis position works to develop collaborative relationships with investigators and site personnel to establish new and ongoing site relationships, as well as support the Strategic Proposal Development staff with feasibility assessments in accordance with feasibility processes and deliverable timelines. The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers the opportunity to have an exciting career in the research of drug and medical device development.
Early Career Clinical Research Opportunities Medpace Holdings IncEarly Career Clinical Research OpportunitiesCincinnati, OHWhen 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.
Clinical Trial Project Manager - Research Nurses Medpace, Inc.Clinical Trial Project Manager - Research NursesCincinnati, 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. Qualifications: BSN is required; 3+ years of Clinical Nurse experience required, research nurse experience preferred; Experience in Phases 1-4; Phases 2-3 preferred; Management of overall project timeline; Strong leadership skills.
NewClinical Research Associate - Ohio Region Bristol-Myers Squibb CoClinical Research Associate - Ohio RegionCleveland, OHRemote$104,680–$126,845 / yearNon-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites.
Research Assistant MothershipResearch AssistantCleveland, OhioLearn more about all the incredible opportunities available at Mothership, where we match you with world renowned clients and jobs, help you develop and grow, enable you with cutting-edge intuitive technology, and so much more! This position plays a crucial role in contributing to cutting-edge projects, gain hands-on experience, and develop your skills in a supportive and innovative workplace.
Research Nurse II/III, Bone Marrow Transplant Cincinnati Children's Hospital Medical CenterResearch Nurse II/III, Bone Marrow TransplantCincinnati, OHDemonstrate critical thinking skills by making appropriate nursing decisions, prioritizing both planned and unplanned events for protocol implementation, and proactively leading efforts to addressing potential and actual problems. Develop a complex plan of care, and effectively prioritize both expected and unanticipated needs for the participants involvement in the research study and make determination of clinical relevance of study procedures and tests.
Clinical Research Coordinator III (RN) *Sign On Bonus* American Oncology NetworkClinical Research Coordinator III (RN) *Sign On Bonus*Columbus, Ohio$26.26–$39.81 / hourClinical Research Coordinator III (RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.
Clinical Research Coordinator III (Rn) *Sign On Bonus* American Oncology NetworkClinical Research Coordinator III (Rn) *Sign On Bonus*Columbus, OH$26.26–$39.81 / hourClinical Research Coordinator III (RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.
Research Assistant II - Experimental Hematology & Cancer Biology - Reynaud Lab Cincinnati Children's Hospital Medical CenterResearch Assistant II - Experimental Hematology & Cancer Biology - Reynaud LabCincinnati, OH$20.57–$25.72 / hourJoin the Reynaud Lab within the Division of Experimental Hematology & Cancer Biology at Cincinnati Children's, where we study how chronic metabolic conditions such as obesity and diabetes influence hematopoietic stem cell function and contribute to blood disorders and leukemia. The Research Assistant will play a key role in supporting laboratory operations, ensuring regulatory and biosafety compliance, managing mouse colonies, and contributing directly to innovative research projects in a collaborative and discovery-driven environment.
Research Assistant, College of Design, Architecture, Art, & Planning University of CincinnatiResearch Assistant, College of Design, Architecture, Art, & PlanningCincinnati, 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 III/IV - Integrated Genomics and Metagenomics Sequencing Cincinnati Children's Hospital Medical CenterResearch Assistant III/IV - Integrated Genomics and Metagenomics SequencingCincinnati, 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.
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.