Registered Dietitian Clinical Research - PRN Professional Case ManagementRegistered Dietitian Clinical Research - PRNCincinnati, OH$42Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career!
Per Diem / PRN Nurse RN - Research / Clinical Research - $40 per hour CommonSpirit Health at HomePer Diem / PRN Nurse RN - Research / Clinical Research - $40 per hourCincinnati, OHLocated in Loveland, OH, CommonSpirit Health at Home has 83 sites of care across 15 states (Arkansas, Arizona, California, Colorado, Illinois, Indiana, Kentucky, Minnesota, Nebraska, North Dakota, Ohio, Oregon, Tennessee, Texas and Washington) and nearly 3,000 employees who support our mission by creating and nurturing healthy communities across the nation. CommonSpirit Health at Home is committed to delivering the best quality care and comprehensive home-based services to the communities we serve by offering quality care and services; home health, hospice care, palliative care, home infusion therapy and supplemental staffing.
Associate Clinical Trial Manager - PhD - Metabolic - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Metabolic - CincinnatiCincinnati, 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 within Metabolic research for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
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.
Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm Medpace, Inc.Associate Clinical Trial Manager - PhD - Oncology, Hematology, RadiopharmCincinnati, 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 related to Oncology, Hematology, and Radiopharm for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - 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 Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office.
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Cincinnati Medpace, Inc.Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - 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 Research experience related to Infectious Disease areas 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.
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.
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 - 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.
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 - 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.
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 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.
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 Trial Project Manager - Research Nurses Medpace, Inc.Clinical Trial Project Manager - Research NursesCincinnati, 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 is required; 3+ years of Clinical Nurse experience required, research nurse experience preferred; Experience in Phases 1-4; Phases 2-3 preferred; Management of overall project timeline; Strong leadership skills.
Clinical Trial Manager BelcanClinical Trial ManagerMason, OHThe CTM role is pivotal for driving robust human testing and clinical trials that are compliant with established governance principles, including ICH-GCP Guidelines. Responsibilities: Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key components of a successful clinical trial.
NewClinical 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.
Clinical Trial Manager Join The CTI TeamClinical Trial ManagerCovington, KentuckyOversight 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.
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.
Experienced Clinical Trial Project Manager Medpace, Inc.Experienced Clinical Trial Project ManagerCincinnati, 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 Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation, and analysis of Phase I - IIa studies.
Clinical Trial Project Manager Medpace, Inc.Clinical Trial Project ManagerCincinnati, 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 Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation, and analysis of Phase I - IIa studies.
Experienced Clinical Trial Project Manager Medpace Holdings IncExperienced Clinical Trial Project ManagerCincinnati, OHMedpace Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation, and analysis of Phase I - IIa studies. Responsible for managing one or more projects according to Sponsor specifications; Coordinate project start-up, maintenance, and close-out activities; Track study status including patient status, case report form status, safety issues, timelines, etc.
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.
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.
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.
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.
Director, Clinical Trial Management - Neuroscience Medpace, Inc.Director, Clinical Trial Management - NeuroscienceCincinnati, 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.
NewSystem Analyst, Healthcare, Clinical Trial System Global Placement FirmSystem Analyst, Healthcare, Clinical Trial SystemCincinnati, OhioAs a key member of our technology team, you will play a critical role in supporting our healthcare clients by translating complex business needs into scalable system solutions. We are seeking a highly skilled and detail-oriented System Analyst with deep expertise in healthcare and clinical trial systems to join our dynamic on-site team.
Clinical Research Project Manager, Department of Neurology & Rehabilitation, Movement University of CincinnatiClinical Research Project Manager, Department of Neurology & Rehabilitation, MovementCincinnati, OHSpecific jobs will include assistance with the coordination and delivery of site protocol training for trial specific procedures, collaborate on the development of related educational materials, facilitate scheduling and leading site readiness calls, help with planning investigators' meetings, contribute to the ongoing monitoring of recruitment and retention, and assist with other ongoing internal and external communication of collaborators. Ensuring IRB compliance throughout the study; reviewing site regulatory and staff documents; overseeing the delegation of authority log process; assisting with eConsent management; facilitating IRB approvals for site Principal Investigator changes; tracking and assisting with the clinical trial agreement process, including any modifications throughout the study; and participating in site readiness calls.
Clinical Informatics Manager Medpace, Inc.Clinical Informatics ManagerCincinnati, OhioQualifications: Bachelor’s degree in informatics, computer science/engineering, biomedical engineering, health information, statistics, data science, life sciences, or a related field; advanced degree preferred; Clinical research, clinical operations, or contract research organization experience; Experience leading, mentoring, or managing technical or analytical team members; Strong programming experience in R and SQL (additional experience with Snowflake and Python is highly valued); Experience developing dashboards, web applications, analytical tools, or other data products for business or operational users; Ability to balance hands-on technical contribution with team leadership, stakeholder management, and strategic planning; Strong analytical thinking, attention to detail, and ability to translate complex operational questions into data-driven solutions; and, Excellent verbal and written communication skills with the ability to work effectively across technical, operational, and clinical teams. 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 Manager Medpace Holdings IncClinical Informatics ManagerCincinnati, OHBachelor's degree in informatics, computer science/engineering, biomedical engineering, health information, statistics, data science, life sciences, or a related field; advanced degree preferred; Clinical research, clinical operations, or contract research organization experience; Experience leading, mentoring, or managing technical or analytical team members; Strong programming experience in R and SQL (additional experience with Snowflake and Python is highly valued); Experience developing dashboards, web applications, analytical tools, or other data products for business or operational users; Ability to balance hands-on technical contribution with team leadership, stakeholder management, and strategic planning; Strong analytical thinking, attention to detail, and ability to translate complex operational questions into data-driven solutions; and, Excellent verbal and written communication skills with the ability to work effectively across technical, operational, and clinical teams. This individual will partner closely with Clinical and Medical Operations, Software Development, IT Architecture, Data Engineering, Business Intelligence, Biostatistics, and other cross-functional stakeholders to translate operational needs into scalable data products.
Manager, Clinical Operations Meridian Bioscience IncManager, Clinical OperationsCincinnati, OHPartner with the Clinical Affairs Director to create and implement the strategic vision for the Clinical Operations team to ensure the high-quality end-to-end management of clinical trials, clinical trial logistics and internal/external biospecimen acquisition. Regularly monitor the overall health of the clinical studies from the study initiation to closure including regular evaluation of key metrics (enrollment, site activation), monitoring and escalation of project risks and mitigation plans when appropriate.
Clinical Manager, Spine Services Mayfield Brain and SpineClinical Manager, Spine ServicesCincinnati, OHMayfield Clinic is looking for a strong clinical leader to serve as our Clinical Manager of Spine Services—an essential role focused on advancing spine care, leading high-performing teams, and driving data-informed operational and quality initiatives across the organization. Must be a graduate of an accredited Nurse Practitioner or Physician Assistant program with a current license to practice nursing in the state of Ohio and Kentucky, or a graduate of an AAPA-accredited school.
Clinical Account Manager - Southeast Region - Cincinnati Rampart IC LLCClinical Account Manager - Southeast Region - CincinnatiCincinnati, OHBacked by peer-reviewed research, real-world studies, and field-tested innovation, Rampart provides comprehensive solutions to protect healthcare teams from the dangers of radiation exposure. As a Clinical Account Manager, you'll be responsible for driving clinical adoption of Rampart products, building new customer relationships, and expanding usage within existing accounts across your assigned territory.
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.
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.
Entry Level Trial Master File (TMF) Specialist Medpace Holdings IncEntry Level Trial Master File (TMF) SpecialistCincinnati, OHProvide 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. 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 Informatics Analyst Medpace, Inc.Clinical Informatics AnalystCincinnati, OhioQualifications: Bachelor’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; Clinical research experience is preferred; 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.
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 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 Supply Chain Project Specialist (Entry) Medpace Holdings IncClinical Supply Chain Project Specialist (Entry)Cincinnati, OHPreferred 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. 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 Research Finance & CTMS Specialist Gastro HealthClinical Research Finance & CTMS SpecialistCincinnati, OHPartner with site staff to ensure completed visits, procedures, stipends, screen failures, unscheduled visits, and protocolrequired activities are properly documented and financially captured. This role will report to the Finance Department, while working closely with Clinical Research leadership,site managers, coordinators, investigators, sponsors, CROs, and external financial partners.
Clinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc.Clinical Research Associate - Clinical Research Coordinator ExperienceCincinnati, OhioRemoteOn-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. 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 Coordinator IV - Bone Marrow Transplantation Cincinnati Children's Hospital Medical CenterClinical Research Coordinator IV - Bone Marrow TransplantationCincinnati, OH$61,401.60–$78,291.20 / yearCreate case report forms (CRFs) in consultation with other team members, as needed, using existing study data information to promote efficient data collection and data entry. Study Conduct/ Clinical Research Practice - Serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials.
Clinical Research Coordinator III Cincinnati Children's Hospital Medical CenterClinical Research Coordinator IIICincinnati, OH$56,784–$62,150.40 / yearServe as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations. Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.
NewClinical Research Coordinator III - Orthopaedics & Sports Medicine Cincinnati Children's Hospital Medical CenterClinical Research Coordinator III - Orthopaedics & Sports MedicineCincinnati, OH$56,784–$62,150.40 / yearServe as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations. Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.
Clinical Research Professional / Clinical Research Professional II, UC Cancer Center University of CincinnatiClinical Research Professional / Clinical Research Professional II, UC Cancer CenterCincinnati, 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 that 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 healthcare professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients.