Pharmacist Clinical Elevance HealthPharmacist ClinicalMason, OH$119,360–$214,848 / yearThe Pharmacist Clinical is responsible for managing the selection and utilization of pharmaceuticals and supports core clinical utilization management programs such as prior authorization, step therapy, quantity limitations and then works with the operational areas to ensure the clinical criteria is implemented correctly. Experienced in cross-mapping clinical codes, optimizing drug-utilization screening rules, and validating clinical data accuracy using the Medi-Span database is highly preferred.
Spring 2027 Clinical Trials Feasibility & Proposals Internship Medpace, Inc.Spring 2027 Clinical Trials Feasibility & Proposals InternshipCincinnati, OhioQualifications: High school diploma or equivalent; Bachelor's degree in progress, in a Life Sciences field; Knowledge of MS Word, Excel, and PowerPoint; Knowledge and organizational skills to perform day-to-day departmental support activities (i.e., shipping, archiving, filing, departmental meeting minutes); Demonstrated ability to maintain applicable database systems; Demonstrated ability to adequately communicate (written and oral) with other employees as necessary; and. Coordinate and provide summary for departmental meetings/conference calls as and when required; Maintain database/spreadsheets and compile reports as necessary to facilitate tracking/documentation of departmental activities; Conduct quality control reviews of departmental documents as necessary; Support other departments on ad hoc projects; and.
Clinical Logistics Intern Medpace Holdings IncClinical Logistics InternCincinnati, OHWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Manage and maintain warehouse organization; Coordinate with vendors to ensure deliveries of products and services align with the needs of the business; Verify all inventory is moved to the correct locations and updated in the Inventory Management System.
Clinical Data Intern - Fall 2026 Medpace, Inc.Clinical Data Intern - Fall 2026Cincinnati, 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 Coder Medpace, Inc.Clinical Data CoderCincinnati, 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 and RN with applicable experience is required, or more advanced clinical degree (including PharmD) is accepted; Strong critical thinking, organizational, and multi-tasking skills required; Experience with using MedDRA and WHO Drug dictionaries preferred; and.
Clinical Informatics Analyst Medpace, Inc.Clinical Informatics AnalystCincinnati, OhioBachelor’s in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to prioritize multiple projects on a sprint schedule; Excellent verbal communication skills; Programming experience in R or Python; Work experience with clinical data; Experience building web applications is preferred (with either Shiny or Streamlit); 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.
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.
NewClinical Supply Chain Project Specialist (PharmD Candidates) Medpace, Inc.Clinical Supply Chain Project Specialist (PharmD Candidates)Cincinnati, OhioQualifications: Must have a Doctor of Pharmacy (PharmD) degree; Ability to escalate; Prioritization of daily, weekly, monthly, and project workloads; Stong communication and problem-solving skills; Ability to effectively collaborate with internal and external colleagues; Provides excellent internal and external customer support; Understand multiple potential solutions; Solid working knowledge of Power Point, Excel, Word; and. Responsibilities: 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.
Clinical Informatics Intern - Summer 2027 Medpace, Inc.Clinical Informatics Intern - Summer 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.
Director, Clinical Trial Management Medpace, Inc.Director, Clinical Trial 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. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add senior-level Directors and established Project Managers to join our Clinical Trial Management Group in Cincinnati, OH, Dallas, TX, Denver, CO.
Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - 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 Gastrointestinal (GI) experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OH Medpace, Inc.Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OHCincinnati, OhioResponsibilities: Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; Interact with the internal project team, Sponsor, study sites, and third-party vendors; Provide oversight and quality control of our internal regulatory filing system; Provide oversight and management of study supplies; Create and maintain project timelines; and. Job Summary: Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
NewClinical Research Project Coordinator - Ophthalmology Medpace, Inc.Clinical Research Project Coordinator - OphthalmologyCincinnati, 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.
NewClinical 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. 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 Assistant Velocity Clinical Research IncClinical Research AssistantCincinnati, OHSummary: The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
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.
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 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.
NewEntry-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. 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.
Early Career Clinical Research Opportunities Medpace, Inc.Early Career Clinical Research OpportunitiesCincinnati, 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.