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.
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.
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 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.
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.
CRC to Site Relationship Coordinator Medpace, Inc.CRC to Site Relationship CoordinatorCincinnati, OhioThis position works to develop collaborative relationships with investigators and site personnel to establish new and ongoing site relationships, as well as support the Strategic Proposal Development staff with feasibility assessments in accordance with feasibility processes and deliverable timelines. The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers the opportunity to have an exciting career in the research of drug and medical device development.
NewEntry-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.
NewEntry-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.
NewTrial 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.
NewEntry-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.
CRC to Site Relationship Coordinator Medpace Holdings IncCRC to Site Relationship CoordinatorCincinnati, OHThis position works to develop collaborative relationships with investigators and site personnel to establish new and ongoing site relationships, as well as support the Strategic Proposal Development staff with feasibility assessments in accordance with feasibility processes and deliverable timelines. The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers the opportunity to have an exciting career in the research of drug and medical device development.
Patient Recruitment and Engagement Manager CPU Medpace Holdings IncPatient Recruitment and Engagement Manager CPUCincinnati, OHImplement 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 TMF Operations Associate Medpace Holdings IncEntry Level TMF Operations AssociateCincinnati, 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 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 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. 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.
MEDICAL DIRECTOR - Oncology Clinical Trials The Christ HospitalMEDICAL DIRECTOR - Oncology Clinical TrialsCincinnati, OHThe Christ Hospital Heart & Vascular Institute three-star rating from The Society of Thoracic Surgeons (STS) for patient care and outcomes in insolated mitral valve replacement and repair (MVRR) surgery and for its patient care and outcomes in coronary artery bypass grafting (CABG). Responsibilities include but are not limited to providing high quality cancer care services, improving access to clinical trials and cancer research in the service area, supporting outreach, leading clinical research and innovations in cancer care and supporting cancer education.
MEDICAL DIRECTOR - Oncology Clinical Trials The Christ Hospital Health NetworkMEDICAL DIRECTOR - Oncology Clinical TrialsCincinnati, OHThe Christ Hospital Heart & Vascular Institute three-star rating from The Society of Thoracic Surgeons (STS) for patient care and outcomes in insolated mitral valve replacement and repair (MVRR) surgery and for its patient care and outcomes in coronary artery bypass grafting (CABG) . Responsibilities include but are not limited to providing high quality cancer care services, improving access to clinical trials and cancer research in the service area, supporting outreach, leading clinical research and innovations in cancer care and supporting cancer education.
Medical Director - Oncology Clinical Trials Christ HospitalMedical Director - Oncology Clinical TrialsCincinnati, OHThe Christ Hospital Heart & Vascular Institute three-star rating from The Society of Thoracic Surgeons (STS) for patient care and outcomes in insolated mitral valve replacement and repair (MVRR) surgery and for its patient care and outcomes in coronary artery bypass grafting (CABG). Responsibilities include but are not limited to providing high quality cancer care services, improving access to clinical trials and cancer research in the service area, supporting outreach, leading clinical research and innovations in cancer care and supporting cancer education.
Associate Director, Clinical Project Management - up to $25K sign-on bonus! Join The CTI TeamAssociate Director, Clinical Project Management - up to $25K sign-on bonus!Covington, KentuckyJob Summary: The Associate Director provides leadership role in facilitating the management of the multiple Phase I-IV clinical research trials across all geographic and functional areas; Responsible for ensuring that direct reports and assigned clinical operation's team members deliver their projects on time, on budget and with an acceptable level of quality. Plan, implement, facilitate and evaluate the full execution of assigned clinical trials; oversee management of multiple clinical trials from the planning phase to the analysis phase for delivery to client; may function as a global lead; may function in day to day operations and/or oversight of trial activities and deliverables.
Senior Clinical Project Manager - up to $20K sign-on bonus! Join The CTI TeamSenior Clinical Project Manager - up to $20K sign-on bonus!Covington, KentuckyThe Senior CPM is expected to be independent but may require consultation and guidance from the trial-assigned Director to ensure successful clinical trial execution and to support other functional team members’ management of daily trial operations. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations.
Clinical Data Coder Medpace Holdings IncClinical Data CoderCincinnati, 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. 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.