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 Safety Manager Medpace, Inc.Clinical Safety ManagerCincinnati, OhioResponsibilities: Line manage, mentor and develop a team of clinical safety professionals; Manage relationships with clients and internal stakeholders by providing expert safety knowledge; Oversee clinical safety case management and aggregate reporting responsibilities of direct reports to ensure client needs are fulfilled to high quality; Create safety management plans dependent upon client; Provide safety review of clinical study documents, including protocols, study reports; and marketing application components. 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 - 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 - 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 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.
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 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 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.
Senior Specialist, Clinical Education THV AR (Midwest US) Edwards Lifesciences CorpSenior Specialist, Clinical Education THV AR (Midwest US)Arkansas, KY$134,000–$190,000 / yearWhat you will need (Required): Bachelor's Degree and a minimum of 5 years clinician experience in intra-operative procedures acquired from Registered Nursing Degree curriculum (RN), or in positions such as Radiologic Technologist (RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS) or related medical device, clinical, or Certification in RDCS (Registered Diagnostic Cardiac Sonographer) within ARDMS (American Registry for Diagnostic Medical Sonography) OR equivalent experience based on Edwards criteria. Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during clinical trial implants, including contingency planning to address unforeseen occurrences in support of assigned clinical investigations.
Science and Engineering Research Program Manager SME Chenega CorporationScience and Engineering Research Program Manager SMEDayton, OHThe Science and Engineering Research Program Manager (SME) will provide subject matter expertise to the Airman Systems Directorate, Airman Biosciences Division (711 HPW/RHB) in support of research and technology evaluation initiatives spanning hazard mitigation, public health, contingency operations, performance enhancement, human systems integration, and clinical aerospace medicine, including aeromedical evacuation. This role supports the Defense Health Program (DHP) Medical Human Performance Portfolio by working directly with the Product Line Lead and Lead Program Manager, as well as R&D personnel and laboratories executing the medical human performance research mission, to advance Air Force Medical Command research interests through the development of individualized high-performance integrated systems and health readiness solutions.
Aprn Business Health St. Elizabeth HealthCareAprn Business HealthErlanger, KYEducation, Credentials, Licenses: Graduate of an accredited Nurse Practitioner or Physician Assistant Program and meets the requirement for certification/re-certification by the National Commission on Certification of Physician Assistants (NCCPA) or master's degree in nursing with National Nurse Practitioner Certification in appropriate specialty area. In accordance with established collaborative practice agreement and evidence-based guidelines, the APRN obtains health histories, performs physical examinations, identifies problems, establishes goals, and formulates comprehensive plans of care for patients and teaches preventive health measures.
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.
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.
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 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 Travel Coordinator Medpace, Inc.Patient Travel CoordinatorCincinnati, 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.
Entry-Level Patient Concierge Coordinator Medpace, Inc.Entry-Level Patient Concierge CoordinatorCincinnati, 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.
Project Coordinator (Site Activation and Maintenance) Medpace, Inc.Project Coordinator (Site Activation and Maintenance)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); 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; Gain exposure to multiple therapeutic areas including but not limited to Oncology/Hematology, Cardiovascular, and Metabolic; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; 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.