392 Results for

Clinical Trial Manager Jobs in Ohio

Jobs

Hudson, OH

li>Sales Enablement & Training: Partner with internal teams and field associates to deliver robust clinical and technical training, ensuring the commercial team can confidently articulate our value proposition to hospital administrators and clinicians.

You will be responsible for translating complex clinical data into compelling value propositions and content and building strong relationships with surgeons and Key Opinion Leaders (KOLs) in the execution of marketing strategy.

11 days ago

Cincinnati, OH

Job Description

We are seeking a Physician or Gastroenterologist with a strong background in digestive health and clinical research to serve as a Principal Investigator for gastroenterology-focused clinical trials at our Cincinnati site. The role includes direct engagement with study participants, supervision of study teams, and collaboration with sponsors and regulators.

1 day ago

Cincinnati, OH

Medpace is delighted to host a Virtual Recruitment Event tailored to candidates studying or holding a PhD in Life Science areas, working within Cardiovascular, Nephrology / Renal or Gastrointestinal (GI), Endocrine, and Metabolic research areas. At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team.

30+ days ago

Cincinnati, OH

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 • Coordinate project meetings and produce quality minutes. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs.

30+ days ago

Cincinnati, OH

p>• 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; • Coordinate project meetings and produce quality minutes.

30+ days ago

Cincinnati, OH

p>• 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 • Coordinate project meetings and produce quality minutes.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

p>Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

• 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; • Coordinate project meetings and produce quality minutes.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

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; • Coordinate project meetings and produce quality minutes. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards.

30+ days ago

Cincinnati, Ohio

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Researchers with Cardiology experience for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office. 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.

29 days ago

Cincinnati, Ohio

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. 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.

30+ days ago

Cincinnati, Ohio

Job Summary: Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office. 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.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

Responsibilities : 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-basedAssociate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

Responsibilities : 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-basedAssociate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.

30+ days ago

Cincinnati, OH

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; Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards.

30+ days ago

Cincinnati, OH

Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

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 Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards.

30+ days ago

Cincinnati, Ohio

p style="margin:0px"> TWP 2024 CRO2024 . Job 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-basedAssociate Clinical Trial Manager (aCTM) position based in our Cincinnati, OH office.

30+ days ago

Cincinnati, OH

30+ days ago

Mason, OH

The 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.

30+ days ago

Cincinnati, Ohio

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 Cardiovascular, Renal, and Gastrointestinal therapeutic areas to join our Clinical Trial Management Group. 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.

30+ days ago

Cincinnati, Ohio

Responsibilities : 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.

30+ days ago

Cincinnati, Ohio

Responsibilities : 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.

30+ days ago

Cincinnati, Ohio

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 in Immunology, Rheumatology, Allergy, and/or Dermatology to join our Clinical Trial Management Group in our Cincinnati, OH office. 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.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

p style="margin:0px"> TWP 2024 CRO2024 . 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.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, Ohio

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. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers with established Clinical Research Nursing backgrounds to join our Clinical Trial Management Group.

30+ days ago

Cincinnati, Ohio

p style="margin:0px"> TWP 2024 CRO2024 . 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.

30+ days ago

Cincinnati, OH

p>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.

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.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, OH

Responsibilities 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 Manage study vendors where applicable Manage site quality and monitoring deliverables Qualifications Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred Experience in Phases 1-4; Phases 2-3 preferred 5+ years as a project/clinical trial manager within a CRO; Management of overall project timeline Bid defense experience, preferred Strong leadership skills Medpace Overview Medpace is a full-service clinical contract research organization (CRO). Cincinnati Perks Cincinnati Campus Overview Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America''s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

30+ days ago

Cincinnati, OH

$56,784–$62,150.40 / year

Serve 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.

30+ days ago

Cincinnati, Ohio

30+ days ago

Cincinnati, OH

Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs. Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

30+ days ago

Cincinnati, OH

30+ days ago

Cincinnati, OH

p>In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company. 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.

30+ days ago

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Clinical Trial Manager job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Clinical Trial Manager Jobs in Ohio

Clinical Marketing Manager ForTec Medical

Physician Gastroenterology - Competitive Salary Green Key Resources

PhD & Postdoctoral Virtual Career Event: Associate Clinical Trial Manager Cardio, Renal, GI, Metabolic June 16 Medpace Holdings Inc

Associate Clinical Trial Manager PhD Cardiovascular Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD / Post Doc Experience Cincinnati, OH Medpace Holdings Inc

Associate Clinical Trial Manager PhD Postdoctoral Infectious Diseases Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Postdoctoral CNS/Neuroscience Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Gastrointestinal (GI) Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Metabolic Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Postdoctoral Ophthalmology Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Postdoctoral Nephrology, Renal Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Immunology Cincinnati Medpace Holdings Inc

Associate Clinical Trial Manager PhD Oncology, Hematology, Radiopharm Medpace Holdings Inc

Associate Clinical Trial Manager - PhD - Cardiovascular - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OH Medpace, Inc.

Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm Medpace, Inc.

Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD - Gastrointestinal (GI) - Cincinnati Medpace, Inc.

Associate Clinical Trial Manager - PhD - Metabolic - Cincinnati Medpace, Inc.

Clinical Trial Project Manager Infectious Diseases Cincinnati Medpace Holdings Inc

Clinical Trial Project Manager Ophthalmology Cincinnati Medpace Holdings Inc

Clinical Trial Project Manager Immunology Cincinnati Medpace Holdings Inc

Clinical Trial Project Manager Cardiovascular, Renal, Gastrointestinal Cincinnati Medpace Holdings Inc

Clinical Trial Project Manager Cincinnati, OH Medpace Holdings Inc

Clinical Trial Project Manager Oncology/Hematology Medpace Holdings Inc

Associate Clinical Trial Manager - PhD - Immunology - Cincinnati Medpace, Inc.

Clinical Trial Project Manager Research Nurses Medpace Holdings Inc

Clinical Trial Manager Belcan

Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - Cincinnati Medpace, Inc.

Clinical Trial Project Manager - Infectious Diseases - Cincinnati Medpace, Inc.

Clinical Trial Project Manager - Oncology/Hematology Medpace, Inc.

Clinical Trial Project Manager - Immunology - Cincinnati Medpace, Inc.

Clinical Trial Project Manager - Ophthalmology - Cincinnati Medpace, Inc.

Clinical Trial Project Manager - Cincinnati, OH Medpace, Inc.

Clinical Trial Project Manager Neuroscience Cincinnati Medpace Holdings Inc

Clinical Trial Project Manager - Research Nurses Medpace, Inc.

Clinical Trial Project Manager - Neuroscience - Cincinnati Medpace, Inc.

Experienced Clinical Trial Project Manager Medpace Holdings Inc

Clinical Trial Project Manager Medpace Holdings Inc

Clinical Trial Project Manager Medpace, Inc.

Experienced Clinical Trial Project Manager Medpace, Inc.

Associate Director, Clinical Trial Management Medpace Holdings Inc

Clinical Research Coordinator III - Neuromuscular Clinical Trial (Neurology) Cincinnati Children's Hospital Medical Center

Associate Director, Clinical Trial Management Medpace, Inc.

Director, Clinical Trial Management Oncology/Hematology Medpace Holdings Inc

Director, Clinical Trial Management Cardiovascular Medpace Holdings Inc

Clinical Trial Associate Trial Master File (TMF) Medpace Holdings Inc

Resume Resources

Similar Job Searches