Clinical Trial Project Manager - Cincinnati, OH Medpace, Inc.Clinical Trial Project Manager - Cincinnati, OHCincinnati, 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 the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Cincinnati, OH .
Clinical Safety Coordinator (Life Sciences Degrees) Medpace, Inc.Clinical Safety Coordinator (Life Sciences Degrees)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. Qualifications: Bachelor’s degree in life/health science including, but not limited to, Microbiology, Biology, Pharmaceutical Science, Chemistry, or related field; Proficient knowledge of Microsoft® Office; Broad knowledge of medical terminology; and.
Executive Director, Clinical Trial Project Management Medpace, Inc.Executive Director, Clinical Trial Project ManagementCincinnati, 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 Trial Project Manager - Ophthalmology - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Ophthalmology - CincinnatiCincinnati, OhioJob Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Ophthalmology to join our Clinical Trial Management Group in our Cincinnati, OH office. 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 Project Coordinator Medpace, Inc.Clinical Project CoordinatorCincinnati, OhioResponsibilities: Provide day-to-day departmental/project support activities, such as maintenance of project-related files and and IRB document preparation and submissions; Data entry into Medpace proprietary systems and Excel spreadsheets; Coordinate and provide minutes for department/project meetings or conference calls; Maintain spreadsheets and compile reports; 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 Trial Project Manager - Neuroscience - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Neuroscience - 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 the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial Management Group in our Cincinnati, OH office.
Clinical Supply Chain Project Specialist (PharmD Candidates) Medpace, Inc.Clinical Supply Chain Project Specialist (PharmD Candidates)Cincinnati, OhioResponsibilities: As a member of CP&S department, support and collaborate in all activities related to investigational productsupply chain; Support CP&S department to translate clinical study protocol into investigational supply chain; Monitor alignment of CP&S timelines with project timelines; Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtually and face to face; and. Qualifications: PharmD; Ability to escalate; Prioritization of daily, weekly, monthly, and project workloads; Stong communication and problem-solving skills; Effectively collaborate with internal and external colleagues; Provide excellent internal and external customer support.
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.
Clinical Trial Project Manager - Immunology - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Immunology - CincinnatiCincinnati, OhioJob Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus in Immunology, Rheumatology, Allergy, and/or Dermatology to join our Clinical Trial Management Group in our Cincinnati, OH office. 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 Clinical Trials Feasibility Coordinator Medpace, Inc.Experienced Clinical Trials Feasibility CoordinatorCincinnati, OhioResponsibilities: Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams; Develop preliminary proposal strategy for site and country selection; Present feasibility results to members of the proposal team to assure 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; Assist with review of work developed by more junior feasibility coordinators; Collaborate with operational team members in preparation for bid defense meetings; and. By working cross functionally with our clinical operations, medical and regulatory submissions teams, as well as through analyzing data from internal and public data sources, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials.
Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - CincinnatiCincinnati, OhioJob Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Cardiovascular, Renal, and Gastrointestinal therapeutic areas to join our Clinical Trial Management Group. 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 Informatics Intern - Spring 2027 Medpace, Inc.Clinical Informatics Intern - Spring 2027Cincinnati, OhioQualifications: Enrollment in Bachelor’s program for informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to work effectively on a sprint schedule; Strong verbal communication skills; Programming experience in R or Python; Clinical research experience is preferred; Experience building web applications is preferred (with either Shiny or Streamlit); and. Responsibilities: Participate in analysts’ evaluation of data needs for assigned projects; Work alongside analysts to contribute innovative data products; Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting; Contribute to algorithm development for descriptive, classification, and predictive operational purposes; and.
Clinical Trial Project Manager - Infectious Diseases - Cincinnati Medpace, Inc.Clinical Trial Project Manager - Infectious Diseases - CincinnatiCincinnati, OhioResponsibilities: Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Cincinnati, OH office.
Clinical Trial Project Manager - Oncology/Hematology Medpace, Inc.Clinical Trial Project Manager - Oncology/HematologyCincinnati, OhioResponsibilities: Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Oncology/Hematology to join our Clinical Trial Management Group in our Cincinnati, OH office.
Medical Assistant, Float Pool, Fulltime, First Shift UC HealthMedical Assistant, Float Pool, Fulltime, First ShiftCincinnati, OHMembers of UC Health include: • UC Medical Center • West Chester Hospital • University of Cincinnati Physicians • UC Health Ambulatory Services (with more than 900 board-certified clinicians and surgeons) • Lindner Center of HOPE • Several specialized institutes, including: • UC Gardner Neuroscience Institute • The University of Cincinnati Cancer Center. UC Medical Center houses Greater Cincinnati's only Level I adult trauma center, which includes the right mix of specialist and medical resources available at a moment's notice for a wide variety of the most complex medical conditions and injuries.
Assistant Staff - Clinical Psychologist Fellow Ochsner Clinic FoundationAssistant Staff - Clinical Psychologist FellowCovington, KentuckyDriven by a mission to Serve, Heal, Lead, Educate and Innovate, coordinated clinical and hospital patient care is provided across the region by Ochsner's 40 owned, managed and affiliated hospitals and specialty hospitals, and more than 100 health centers and urgent care centers. The Ochsner Health fellowship will reside within the Department of Psychiatry which will provide opportunities to work and collaborate with psychiatrists, medical psychologists, clinical psychologists, psychiatric nurse practitioners, physician assistants, licensed professional counselors, and social workers.
Entry-Level TMF Operations Associate Medpace, Inc.Entry-Level TMF Operations AssociateCincinnati, 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. Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and.
Entry-Level TMF Administrator Medpace, Inc.Entry-Level TMF AdministratorCincinnati, 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. Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and.
Patient Recruitment and Engagement Manager-CPU Medpace, Inc.Patient Recruitment and Engagement Manager-CPUCincinnati, OhioResponsibilities: Implement various recruitment strategies for clinical research studies at Medpace Clinical Pharmacology Unit (MCPU); Work effectively with physicians, patient advocacy and specialized community groups to support and increase participant enrollment. 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.
Entry-Level Trial Master File (TMF) Specialist Medpace, Inc.Entry-Level Trial Master File (TMF) 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.