NewMarket Leader SavATreeMarket LeaderMaineville, OHFull timeli>Partner with the sales team to identify new business opportunities, expand existing client relationships, and grow all service lines including Tree Care, Plant Health Care, Lawn Care, and Commercial Services. This role combines strategic leadership with hands on operational execution and offers the opportunity to lead a business that makes a lasting impact on customers, employees, and the communities we serve.
SVP - Consumer Bank Data Analytics, CX and Research Leader U.S. BancorpSVP - Consumer Bank Data Analytics, CX and Research LeaderCincinnati, OH$214,795–$252,700 / yearSuccess in this role depends on strong partnership with Consumer Banking Product, Marketing, Sales, Digital, and Technology teams to solve complex business problems through analytics, research, and CX insights. In addition, certain positions may also be subject to the requirements of FINRA, NMLS registration, Reg Z, Reg G, OFAC, the NFA, the FCPA, the Bank Secrecy Act, the SAFE Act, and/or federal guidelines applicable to an agreement, such as those related to ethics, safety, or operational procedures.
Senior Manager 1: Research Leader - Deloitte Center for Health Solutions Deloitte Touche Tohmatsu LtdSenior Manager 1: Research Leader - Deloitte Center for Health SolutionsOH$124,600–$255,900 / yearDeloitte's Center for Health Solutions (DCHS) is seeking a Senior Research Leader to drive innovative thought leadership, support our teams, serve our clients, develop impactful collaborations in the market, and elevate the voice of Deloitte in life sciences and the health care industry. Help support and enhance an always-on distribution system (segmented audiences, executive moments that matter, enablement packaging, and digital/multimedia assets) so business leaders receive relevant and timely insights when they can act.
Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate)Cincinnati, OHRemotep>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 Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Must have a minimum of a Bachelor's degree in a health or science related field Experience as a Clinical Research Coordinator (minimum 1 year) Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely 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 Must be detail-oriented and efficient in time management.
Senior Alt-PNT Research Engineer University of DaytonSenior Alt-PNT Research EngineerDayton, OHThis position will be responsible for working, as part of a diverse and skilled technical team, to lead and explore new development work for Alternative PNT projects across the Department of War (DoW), as well as leading teams of engineers to develop novel solutions. Preferred Qualifications: While not everyone may possess all of the preferred qualifications, the ideal candidate will bring many of the following: Doctoral degree in Electrical Engineering, Computer Engineering, Computer Science, or related field.
Design Research & Experience Strategist Kaleidoscope Animations (Inactive)Design Research & Experience StrategistCincinnati, OHp>We are seeking a Design Research & Experience Strategist to lead and grow our research practice while expanding the role of research across product, service, brand, consumer, medical, and digital experience opportunities. The ideal candidate is a self-starter who can identify opportunities, build structure where ambiguity exists, and translate user understanding into actionable strategies that inform design, innovation, and business decisions.
Research Associate, Department of Internal Medicine, Division of Infectious Diseases University of CincinnatiResearch Associate, Department of Internal Medicine, Division of Infectious DiseasesCincinnati, OHApply a thorough understanding of the scientific principles underlying the research, including experimental design, immunological mechanisms, assay sensitivity and specificity, and data analysis in order to critically interpret experimental results, identify sources of variability or error, and systematically troubleshoot, optimize, and modify procedures and techniques to ensure rigor, reproducibility, and successful study outcomes. Maintain accurate and detailed records of all laboratory work and experiments, including creation of databases for new studies, expansion of databases for ongoing projects, development of datasets for statistical analysis, and implementation of quality control measures.
Research Associate, College of Design, Architecture, Art, & Planning University of CincinnatiResearch Associate, College of Design, Architecture, Art, & PlanningCincinnati, 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.
NewScientific Writer & Research Development Specialist, UC Cancer Center University of CincinnatiScientific Writer & Research Development Specialist, UC Cancer CenterCincinnati, OHThis position supports faculty investigators in the development of competitive grant proposals, contributes to the preparation and management of the Cancer Center Support Grant (CCSG) and related reports, and assists with strategic planning, monitoring, evaluation, and reporting activities. 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."
Open Rank-Associate or Full Professor, College of Nursing, Office of Research and PhD Education University of CincinnatiOpen Rank-Associate or Full Professor, College of Nursing, Office of Research and PhD EducationCincinnati, OHReal Work-Life BalanceUC prioritizes work-life balance with a generous time-off policy includingVacation and sick time11 paid holidays and additional end-of-year paid time off Winter Season Days6 weeks of paid parental leave for new parentsAdditional Benefits IncludeCompetitive salary based on experienceComprehensive health coverage medical dental vision prescriptionFlexible spending accounts & wellness programsProfessional development & mentorship opportunities. UCs 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.
Student Success Analyst, Institutional Research & Academic Analytics University of CincinnatiStudent Success Analyst, Institutional Research & Academic AnalyticsCincinnati, OHul>Three (3) years of relevant experience in data analysis or applied analytics, including demonstrated proficiency in R or another analytical programming language (Python, SAS, or SQL) and experience developing reports or models from large datasets. Partner with academic and administrative units to deliver practitioner-facing analytics, presenting findings in formats that are accessible, actionable, and appropriate for non-technical audiences including advisors, program staff, and college leadership.
Clinical Research Project Manager, Department of Neurology & Rehabilitation, STEP University of CincinnatiClinical Research Project Manager, Department of Neurology & Rehabilitation, STEPCincinnati, 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.
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.
NewPrincipal Mechanical Research Engineer University of DaytonPrincipal Mechanical Research EngineerDayton, OHCandidate must be able to utilize Photon Doppler Velocimetry (PDV) measurement techniques to obtain material properties and surface velocities post-impact. Candidate will market their PDV measurement techniques to gain new customers and expand Impact Physics Group capabilities.
Actuarial Research Analyst - Financial Institution Services Great American Insurance CompanyActuarial Research Analyst - Financial Institution ServicesCincinnati, OHTarget clients include commercial banks, credit unions, finance companies, buy-here pay-here dealers and leasing and rental concerns. At Great American, we value and recognize the benefits derived when people with different backgrounds and experiences work together to achieve business results.
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 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.
Dir, Research Science Silfex IncDir, Research ScienceOHThis role builds and guides a high-performing team of scientists and engineers, partners closely with Operations, Quality, and Product Management, and drives a portfolio of current and long-term R&D initiatives aligned to business strategy. Silfex Inc., A Lam Research Company is the leading provider of precision silicon components used to make and operate semiconductor tools, which enable the trillion-dollar global electronics industry.
Product Owner - Advanced Analytics & Research Great American Insurance CompanyProduct Owner - Advanced Analytics & ResearchCincinnati, OHIT Services can include a wide range of activities such as: • Software development • Data management • Cloud services • IT security • Network security • Technical support • Establishing and overseeing access rights • Procuring and maintaining equipment or software • Managing the infrastructure • Defining security procedures. Experience building customer-facing AI applications (internal customers such as underwriting, claims, actuarial, and analytics teams), including conversational UX patterns, RAG grounding, structured outputs, and feedback loops that build user trust.
Research Associate-Cyber Library, Ohio Cyber Range Institute, School of Information Technology, CECH University of CincinnatiResearch Associate-Cyber Library, Ohio Cyber Range Institute, School of Information Technology, CECHCincinnati, OH$57,000–$67,000 / yearOCRI administers the Ohio Cyber Range as a state-wide tool that supports programming for K-20 courses and events; full-spectrum training opportunities, including incident response teams; industry workforce and economic development; cyber security research; as well as government agency support among other programs. The SoIT is home to several centers including an NSA/DHS 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.
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. .
Clinical Research Documentation Administrator (TMF) Medpace, Inc.Clinical Research Documentation Administrator (TMF)Cincinnati, Ohiop style="margin:0px"> . 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. *This position is fully office-based in Cincinnati, OH.
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.
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.
Clinical Research Associate (Physical Therapist Candidates) Medpace Holdings IncClinical Research Associate (Physical Therapist Candidates)Cincinnati, OHp>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; 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 Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. 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 Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Clinical Research Associate (PhD Candidates) Medpace Holdings IncClinical Research Associate (PhD Candidates)Cincinnati, OHp>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 Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. 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 Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Clinical Research Associate Cincinnati, OH (Entry Level) Medpace Holdings IncClinical Research Associate Cincinnati, OH (Entry Level)Cincinnati, OHp>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 Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. 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 Must be detail-oriented and efficient in time management.
Investment Research Analyst Great American Insurance CompanyInvestment Research AnalystCincinnati, OHli>Generally, 3+ years of experience in credit research, leveraged finance, or corporate banking; Formal bank credit training program completion is highly desirable. Responsibilities include reviewing financial statements and audits to assess financial health, monitoring market trends, and staying current on company performance to evaluate credit worthiness.
Advanced Analytics & Research Specialist Great American Insurance CompanyAdvanced Analytics & Research SpecialistCincinnati, OHp>• Evaluate emerging AI technologies (agents, workflows, RAG architectures, tool-augmented LLMs) against business requirements and enterprise constraints • Build rapid prototypes that demonstrate feasibility and business value to stakeholders • Document findings thoroughly, both successes and failures, to inform enterprise AI strategy • Partner with Enterprise Architecture to ensure prototypes align with API-first principles and can transition to production systems • Enable business-side data science capabilities: self-service analytics sandboxes, Python environments, and dashboards that dont require IT intervention • Implement and evaluate agent frameworks, Model Context Protocol (MCP) integrations, and AI orchestration patterns • Communicate complex technical concepts to business stakeholders and executives • Mentor team members and contribute to a culture of continuous learning. Please provide: • Resume highlighting relevant AI/ML project experience and outcomes achieved • Examples of prototypes, proofs-of-concept, or projects youve built (GitHub, portfolio, or descriptions) • Brief description of a technology you evaluated that didnt work out, and what you learned • References who can speak to your technical capabilities and collaboration style.
Research Scientist James Hardie Building Products IncResearch ScientistOH$85,000–$90,000 / yearDirector R&D - Decking, Railing & Accessories Product Development, is expected to be a recognized key and critical contributor providing technical direction for major projects in developing decking products with high levels recycled PVC resin in the formulations. James Hardie will comply with any applicable state and local laws regarding employee leave benefits, including, but not limited to providing time off pursuant to the Colorado Healthy Families and Workplaces Act, in accordance with its plans and policies.
Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic Medpace, Inc.Clinical Research Project Coordinator - Cardiovascular, Renal, MetabolicCincinnati, 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 - Ophthalmology Medpace, Inc.Clinical Research Project Coordinator - OphthalmologyCincinnati, Ohio
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. 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 - Neuroscience Medpace, Inc.Clinical Research Project Coordinator - NeuroscienceCincinnati, 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 - Oncology Medpace, Inc.Clinical Research Project Coordinator - OncologyCincinnati, Ohio
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. .
Clinical Trial Project Manager - Research Nurses Medpace, Inc.Clinical Trial Project Manager - Research NursesCincinnati, Ohiop style="margin:0px"> . Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers with established Clinical Research Nursing backgrounds to join our Clinical Trial Management Group.
Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.Experienced Clinical Research Associate - Hematology/OncologyCincinnati, Ohiop style="margin:0px"> . Candidates 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.
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. .
Clinical Research Project Coordinator - Immunology Medpace, Inc.Clinical Research Project Coordinator - ImmunologyCincinnati, 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. .
Entry-Level Research Project Coordinator Medpace, Inc.Entry-Level 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. .
Director of Programs 2 - Research & Advanced Design Northrop Grumman CorpDirector of Programs 2 - Research & Advanced DesignBeavercreek, OH$242,100–$363,100 / yearp>Success in this role will be measured by meeting or exceeding R&AD AOP awards for the existing portfolio, increasing portfolio CAGR for new opportunities, achieving a > 1.0 portfolio book-to-bill, meeting partner NGAS Division award targets, and minimizing schedule variance on product and schedule deliveries. Sets & drives strategy for a broad set of Business Group or Sector initiatives Is empowered to make decisions and is accountable for results that significantly impact sector AOP & LRSP goals (key sector or Company initiatives) Decisions are critical & direct risk/reward implications for sector.
Sr Research Engineer - Polymer Materials James Hardie Building Products IncSr Research Engineer - Polymer MaterialsOH$120,000–$135,000 / yearp>James Hardie will comply with any applicable state and local laws regarding employee leave benefits, including, but not limited to providing time off pursuant to the Colorado Healthy Families and Workplaces Act, in accordance with its plans and policies. James Hardie is the industry leader in exterior home and outdoor living solutions, with a portfolio that includes fiber cement, fiber gypsum, composite and PVC decking and railing products.
Clinical Research Project Coordinator Neuroscience Medpace Holdings IncClinical Research Project Coordinator NeuroscienceCincinnati, OHp>• 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; • 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, OHp>• 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; • 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.
Entry Level Research Project Coordinator Medpace Holdings IncEntry Level Research Project CoordinatorCincinnati, OHp>• 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; • 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 Oncology Medpace Holdings IncClinical Research Project Coordinator OncologyCincinnati, OHp>• 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; • 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 Infectious Disease Medpace Holdings IncClinical Research Project Coordinator Infectious DiseaseCincinnati, OHp>• 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; • 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 Gastrointestinal/GI Medpace Holdings IncClinical Research Project Coordinator Gastrointestinal/GICincinnati, OHp>• 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; • 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.
Cincinnati Clinical Research Project Coordinator Medpace Holdings IncCincinnati Clinical Research Project CoordinatorCincinnati, OHp>• 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; • 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.