Procurement Manager Integrated Resources, IncProcurement ManagerCincinnati, OhioContractorAdditional responsibilities will include: • Partnering with key stakeholders which include the areas of: new product development teams, life cycle engineering, current Make sites-Operations, Product Management Engineering, Quality, Finance, and Planning, to insure that the Electro Mechanical Supply Chain incorporates strategies which support the key elements of Product Quality, Delivery and Cost Efficiency. • Leading strategic direction and execution in sourcing Electro-Mechanical Category for the segment to ensure optimal mix of cost and cycle time, while continually guaranteeing required levels of quality.
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.
Senior Clinical Research Coordinator - DDBP, Froehlich Lab Cincinnati Children's Hospital Medical CenterSenior Clinical Research Coordinator - DDBP, Froehlich LabCincinnati, OH$74,297.60–$94,744 / yearThe Froehlich Lab in the Division of Developmental and Behavioral Pediatrics conducts clinical research focused on improving outcomes for children with ADHD and other developmental-behavioral conditions, including those with complex medical, developmental, and psychosocial needs. The Senior Clinical Research Coordinator will provide leadership for clinical research studies, overseeing study operations, regulatory compliance, participant engagement, data management, and study execution.
Clinical 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.
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.
Study Start-Up Project Manager Medpace, Inc.Study Start-Up Project ManagerCincinnati, OhioEffectively lead others in a matrix environment; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Serve as a Sponsor point of contact for start-up and regulatory submissions items; Review pertinent regulations to develop proactive solutions to start-up challenges; Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits; Contribute to the growth and development of departmental staff, processes and systems. Qualifications: Bachelor's degree required, advanced degree in Life Sciences preferred; 5+ years of experience in clinical research, preferably at a CRO in Study Start-Up or as a Research Manager at a study site; Project management experience and demonstrated role in developing others; and.
Clinical Research Associate - Cincinnati, OH (Entry-Level) Medpace, Inc.Clinical Research Associate - Cincinnati, OH (Entry-Level)Cincinnati, 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. 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.
AI Project Manager Medpace, Inc.AI Project ManagerCincinnati, OhioResponsibilities: Working across Medpace on behalf of the Chief AI Office, the individual will manage and provide accountability for day-to-day operations of the overall AI project list and ensure good communications with teams through meetings such as the AI deep dive Tech and AI working group; Serve as primary AI contact for oversight of operational project-specific issues and work with teams on project deliverables; Support the CAIO with global initiatives such as analysis and expansion of Microsoft Co-pilot capabilities by leading the project to communicate the latest advances to the AI working group and to collect proof points of benefits for presentation to the executive committee; Support the CAIO with any requests from the organization communicating to the CAIO for questions and answers concerning the use of AI; Maintain in depth knowledge of AI projects and an understanding of the latest AI capabilities; Work with the CAIO to explore additional AI projects across Medpace and in the communication and dissemination of those projects to various stakeholders; Provide cross-functional oversight of internal project team members and deliverables; Develop operational project plans; Manage risk assessment and execution. Qualifications: Bachelor’s degree or higher in a technical, business, or healthcare field; Knowledge of clinical research is preferred; 1+ years of experience as a technical or healthcare project manager; Experience in the management of overall project roadmaps and timeline; and.
eClinical Project Manager Medpace, Inc.eClinical Project ManagerCincinnati, OhioQualifications: Bachelor’s degree and prior eClinical experience; including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor; General knowledge of technology trends and system / application development; Possess excellent organizational, prioritization, and time management skills; A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies. Responsibilities: Manage multiple projects from am eClinincal/eCOA perspective; Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments; Coordinate overall eClinical activities by serving as primary contact for the sponsor; Monitor study timelines in relation to clinical trial needs; Attend face to face sponsor meetings and Investigator Meetings.
Feasibility Manager Medpace, Inc.Feasibility ManagerCincinnati, OhioConduct feasibility assessments for strategic or high priority clients in support of proposal development for new business opportunities, and provide high quality, accurate feasibility data to internal and external teams; Present feasibility results to members of the proposal team to ensure correct assumptions were applied and strategy is in line with our therapeutic and operational experience; As needed to support feasibility strategy, coordinate outreach to investigative sites to obtain indication and protocol specific feedback; Provide management, mentoring, training and guidance to more junior members of the team, including entry level feasibility coordinators; Work collaboratively with project teams to support preparation for proposal documents and bid defense meetings; 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.
Project Finance Account Manager Medpace, Inc.Project Finance Account ManagerCincinnati, OhioQualifications: Bachelor's degree in business, finance, or accounting; 5 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 working knowledge of drug development services; Excellent analytical, as well as written and oral communication, skills; Excellent computer skills with a strong knowledge of Microsoft® Excel; and. Responsibilities: Prepare and follow through on bids for new business; Oversee financial and contractual performance of Sponsor projects; Maintain a strong relationship with the customer during an ongoing clinical trial; Perform financial analysis and reporting; Oversee client requests for proposals; Develop change-in-scope documents for ongoing trials; Customize pricing according to client requirements; Develop study metrics; and.
Finance Account Manager Medpace, Inc.Finance Account ManagerCincinnati, OhioQualifications: Bachelor's degree in business, finance, or accounting; 5 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 working knowledge of drug development services; Excellent analytical, as well as written and oral communication, skills; Excellent computer skills with a strong knowledge of Excel; and. Responsibilities: Prepare and follow through on bids for new business; Oversee financial and contractual performance of Sponsor projects; Maintain a strong relationship with the customer during an ongoing clinical trial; Perform financial analysis and reporting; Oversee client requests for proposals; Develop change-in-scope documents for ongoing trials; Customize pricing according to client requirements; Develop study metrics; and.
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.
Clinical Research Coordinator II- Ophthalmology Cincinnati Children's Hospital Medical CenterClinical Research Coordinator II- OphthalmologyCincinnati, OH$24.46–$27.73 / hourStudy 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.
NewClinical Research Coordinator - Pharmacology Cincinnati Children's Hospital Medical CenterClinical Research Coordinator - PharmacologyCincinnati, OHStudy 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.
AI Project Manager Medpace Holdings IncAI Project ManagerCincinnati, OHWorking across Medpace on behalf of the Chief AI Office, the individual will manage and provide accountability for day-to-day operations of the overall AI project list and ensure good communications with teams through meetings such as the AI deep dive Tech and AI working group; Serve as primary AI contact for oversight of operational project-specific issues and work with teams on project deliverables; Support the CAIO with global initiatives such as analysis and expansion of Microsoft Co-pilot capabilities by leading the project to communicate the latest advances to the AI working group and to collect proof points of benefits for presentation to the executive committee; Support the CAIO with any requests from the organization communicating to the CAIO for questions and answers concerning the use of AI; Maintain in depth knowledge of AI projects and an understanding of the latest AI capabilities; Work with the CAIO to explore additional AI projects across Medpace and in the communication and dissemination of those projects to various stakeholders; Provide cross-functional oversight of internal project team members and deliverables; Develop operational project plans; Manage risk assessment and execution. Bachelor's degree or higher in a technical, business, or healthcare field; Knowledge of clinical research is preferred; 1+ years of experience as a technical or healthcare project manager; Experience in the management of overall project roadmaps and timeline; and.
Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity Medpace, Inc.Home-Based Experienced CRA (Clinical Research Associate)- Bonus/EquityCincinnati, OhioRemoteOn-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. 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.
Project Manager, Central Labs Thermo Fisher ScientificProject Manager, Central LabsHighland Heights, KentuckyRemoteGuide and support workflow of Project Managers and Set-up Administrators with special attention to training junior personnel, perform as a mentor and trainer for (newly assigned) Project Managers, identify areas for development and efficiencies in performing tasks, author, review, revise and implement relevant procedural documents, and serve as a backup for the Associate Director PM when needed. The Project Manager, Central Labs monitors and manages all aspects of designated clinical trial protocols in Global Central Labs and is accountable for overall project performance and client’s satisfaction by meeting their needs and expectations through the life cycle of the assigned clinical trials.
Registered Nurse Care Manager Cincinnati Children's Hospital Medical CenterRegistered Nurse Care ManagerCincinnati, OH$81,723.20–$104,208 / yearLeads the coordination of care, setting priorities and encouraging the appropriate use and timeliness of health care services Facilitates a smooth transition of care by ensuring that key components of the plan of care and/or patient needs are communicated to subsequent care providers across the continuum. As a Registered Nurse Navigator, you will play a vital role in managing the care of a complex patient population while collaborating with physicians, advanced practice providers, genetic specialists, researchers, and multidisciplinary teams to ensure seamless, comprehensive care.
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.