Quality Technician I Glanbia plcQuality Technician ISharonville, OHTeamwork - balances team and individual responsibilities; exhibits objectivity and openness to others views; gives and welcomes feedback; contributes to building a positive team spirit; puts success of team above own interests; able to build morale and group commitments to goals and objectives; supports everyones efforts to succeed. Maintain Customer Specifications in ERP system and Batch Works systems to ensure consistent communication of specifications to customers and equivalence of the two specification management systems.
Health Care Marketing Strategy Manager Deloitte Touche Tohmatsu LtdHealth Care Marketing Strategy ManagerCincinnati, OH$163,400–$322,100 / yearWe are looking for practitioners who will work alongside Health Care organization leadership teams to drive business value through the design and delivery of marketing strategies that connect customer insight to business impact. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Health Care Marketing Strategy Senior Manager Deloitte Touche Tohmatsu LtdHealth Care Marketing Strategy Senior ManagerCincinnati, OH$198,700–$391,600 / yearThe Health Care Marketing Strategy Senior Manager is a client-facing consulting leader responsible for balancing oversight and expert guidance across multiple high-impact marketing strategy engagements while driving pipeline and sales generation activities for Health Care clients. We are looking for practitioners who will work alongside Health Care organization leadership teams to drive business value through the design and delivery of marketing strategies that connect customer insight to business impact.
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.
Adjunct Instructor, Anatomy & Physiology/Pharmacology, UC Blue Ash College University of CincinnatiAdjunct Instructor, Anatomy & Physiology/Pharmacology, UC Blue Ash CollegeCincinnati, OHJob Description Apply now Job Title Adjunct Instructor Anatomy & PhysiologyPharmacology UC Blue Ash College Posting Start Date 21126 Work Arrangement Onsite Current UC employees must apply internally via SuccessFactorsYou are invited to submit an application to be included in the general pool of candidates from which qualified faculty roles will be filled. The college is a recipient of the Cincinnati Business Courier 2021 Best Places to Work award and in 2025 earned national recognition for student opportunity and success being named Opportunity Colleges and Universities a distinction awarded to institutions that serve as national models for advancing student success.
Clinical Research Project Coordinator - Oncology Medpace, Inc.Clinical Research Project Coordinator - OncologyCincinnati, 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. 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 Application Support Medpace, Inc.Clinical Application SupportCincinnati, OhioResponsibilities: Interpret 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. Qualifications: 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.
Entry-Level Project Coordinator (Study Start-Up) Medpace, Inc.Entry-Level Project Coordinator (Study Start-Up)Cincinnati, OhioResponsibilities: Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collaborate with Medpace internal employees including CTMs, CRAs, and Contract Specialists to manage study start-up process. 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.
Experienced Study Start-Up Coordinator Medpace, Inc.Experienced Study Start-Up CoordinatorCincinnati, OhioResponsibilities: Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB); Maintain timelines for study start-up through both internal and external collaboration; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and. Qualifications: Bachelor's degree required (preferably in a Life Sciences field); 1-5+ years of prior experience as a study coordinator or within the pharmaceutical industry specializing in study start-up is required; Excellent organizational and prioritization skills; Knowledge of Microsoft Office; and.
Clinical Data Coordinator (PhD/PharmD) Medpace, Inc.Clinical Data Coordinator (PhD/PharmD)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. 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 Data Coordinator - Entry Level Medpace, Inc.Clinical Data Coordinator - Entry LevelCincinnati, 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.
Finance Account Analyst - Laboratory Operations Medpace, Inc.Finance Account Analyst - Laboratory OperationsCincinnati, 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 for Medpace Laboratories; Provides financial input for response to requests for information (RFIs), and ensures coordination of all information with other relevant Medpace personnel as required; Understand existing customer or potential customer’s business, pipeline, and opportunities in order to approach customer with confidence and knowledge; 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; Build relationships within customer’s organization in order to generate new business opportunities and to develop partnership atmosphere; 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 Life Sciences or Finance/Accounting/Business; 0-3 years of laboratory experience or in the conduct of clinical research and/or contract management/pricing; Basic knowledge of medical terminology and a working knowledge of drug development services desired; Excellent analytical, written and oral communication skills; and.
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. 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.
Digital Marketing Specialist - Patient Recruitment Medpace, Inc.Digital Marketing Specialist - Patient RecruitmentCincinnati, OhioResponsibilities: Develop meaningful content for creative materials that target a global audience of patients, caregivers, research site staff, and physicians; Manage media campaigns and develop recruitment funnels including use of Google Ads, Meta, radio, programmatic, and other digital advertising channels; Translate complex scientific concepts into simplified and approachable content; Manage online community, influencer, and advocacy support opportunities; Develop digital tools focused on patient engagement and awareness of the study in support of online engagement efforts; Review and analyze patient recruitment advertisement vendor campaigns and results; Work with preferred video development vendors to product site and patient training and educational videos; Work closely with graphic designers to develop an effective study brand and suite of materials; 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.
Associate Clinical Trial Manager - PhD - Cardiovascular - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Cardiovascular - CincinnatiCincinnati, 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. Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Researchers with Cardiology experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
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. 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.
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.
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. 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.
Data Standard Analyst - Biostatistics Team Medpace, Inc.Data Standard Analyst - Biostatistics TeamCincinnati, 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.
Trial Master File Specialist Medpace, Inc.Trial Master File SpecialistCincinnati, OhioResponsibilities: Provide guidance and support to study team members and sponsors regarding TMF management; Initiate and manage TMF Specifications based on scope of work, protocol, and other core documents working with functional area leads and sponsor contacts; Set up and maintain study specific TMF folder structure; Support CTMs with review of TMF Plans as required; Support study team(s) during periodic TMF QCs by assisting with report development and metric reporting; Report on TMF Health to Sponsors and CTMs; Contribute to audit/inspection readiness activities by reviewing the TMF, TMF Specifications, and TMF Plans for accuracy, consistency, and completeness; Train and mentor other TMF staff; 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.