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.
Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - 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 Nephrology & Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) in our Cincinnati, OH office.
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.
Director, Clinical Trial Management - Cardiovascular Medpace, Inc.Director, Clinical Trial Management - CardiovascularCincinnati, 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 Supply Chain Project Specialist (Entry) Medpace, Inc.Clinical Supply Chain Project Specialist (Entry)Cincinnati, OhioPreferred majors: Life Sciences, Supply Chain Management, Operations Management, Business, Math; Minimum 1-year industry experience is preferred; Ability to escalate; Prioritization of daily, weekly, monthly, and project workloads; Strong communication and problem-solving skills; Ability to provide excellent internal and external customer support; Must be flexible and able to work in a risk-based environment and understand multiple potential solutions; Solid working knowledge of Power Point, Excel, Word; and. Responsibilities: As a member of Clinical Packaging and Supplies (CP&S) department you will: Support and collaborate in all activities related to investigational product supply chain, potentially including manufacturing, packaging, labeling, storage, and distribution; Monitor alignment of CP&S timelines with project timelines; Attend teleconfrences with internal Medpace teams, Sponsors, and/or Vendors and communicate/present both virtual and face to face; and.
Clinical Nurse Medpace, Inc.Clinical NurseCincinnati, OhioResponsibilities: Provide nursing coverage as required for the Medpace Clinical Pharmacology Unit according to the study protocol, applicable SOPs, and Good Clinical Practice; Perform and document clinical procedures (e.g., vital signs, intravenous (IV) insertions, venipunctures, laboratory tests, electrocardiograms) as appropriate to specific needs of study and individual subjects; Responsible for accurate and safe administration/dispensation of medications according to protocol; Assess and document adverse events; 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.
Director, Clinical Trial Management - Oncology/Hematology Medpace, Inc.Director, Clinical Trial Management - Oncology/HematologyCincinnati, 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.
Associate Director, Clinical Trial Management Medpace, Inc.Associate Director, Clinical Trial ManagementCincinnati, OhioJob 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 across our US offices. 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 - Immunology - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Immunology - CincinnatiCincinnati, OhioJob Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Immunology, Rheumatology, Allergy or Dermatology areas for a full-time, office-based Associate Clinical Trial Manager (aCTM) position based 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.
Entry Clinical Trials Feasibility Specialist Medpace, Inc.Entry Clinical Trials Feasibility SpecialistCincinnati, 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 project teams with 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.
Inpatient Psychiatrist, Department of Psychiatry & Behavioral Neuroscience University of CincinnatiInpatient Psychiatrist, Department of Psychiatry & Behavioral NeuroscienceCincinnati, OHThe Department of Psychiatry and Behavioral Neuroscience is dedicated to high quality medical student, resident, and fellow education, excellence in patient care, and advancing the science in psychiatry and behavioral neurosciences through clinical trials and ongoing collaborative research. The department supports clinical care and career development in multiple disciplines, including general psychiatry, addiction psychiatry, forensic psychiatry, consultation-liaison psychiatry, geriatric psychiatry, and neuromodulation including electroconvulsive therapy and transcranial magnetic stimulation.
Clinical Laboratory Data Coordinator Medpace Holdings IncClinical Laboratory Data CoordinatorCincinnati, OHMaintain daily routine maintenance over assigned studies via edits, data queries, data changes, and Data Management sample management; Manage and resolve processing errors and inconsistencies daily to ensure client commitment is met (i.e., problem samples, missing samples, misrouted samples, sample testing); Ensure continuous maintenance/follow-up over study assignments to prepare for study timelines (i.e., data locks, study close-out, etc.); Communicate with other internal functional groups and external clients (i.e., sites, vendors, sponsors) on study progress; 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 Manager CTI Clinical Trial Services, Inc.Clinical Trial ManagerCovington, KYFull timeOversight of key clinical monitoring metrics, including but not limited to: Visits scheduled per CTMP, Monitoring Visit Reports (MVR) and associated correspondence timelines, Action Items (AI), query resolution, and other quality metrics, to ensure they are met and followed-up on as necessary. Bachelor's Degree or higher in allied health field such as nursing, pharmacy, or health / natural science, or RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources.
Phlebotomist Second Shift Medpace Holdings IncPhlebotomist Second ShiftCincinnati, OHAssist with study participant screening, admission, orientation, conduct, and discharge; Demonstrate technical skills in phlebotomy, laboratory specimen collection, electrocardiogram placement, vital signs, and other protocol-related procedures; Assess, document, and notify appropriate project team members of study participant adverse events in timely manner; Assist other clinical staff with study-related duties (e.g., laboratory draws, electronic data capture entry, queries, follow-up appointments); 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.