Medpace
Clinical Trial Project Manager - Oncology/Hematology (Sign-On Bonus Eligible)
Medpace, Denver, Colorado, United States, 80285
Clinical Trial Project Manager - Oncology/Hematology (Sign-On Bonus Eligible)
Job Locations
United States-OH-Cincinnati | United States | United States-TX-Irving (Dallas) | United States-CO-Denver
Category
Clinical Trial Management
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. We have just expanded our campus in Cincinnati and have offices in Dallas and Denver, and provide remote flexibility with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.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; andManage site quality, including direct supervision of project Clinical Research Associates 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-
required for home-based;Management of overall project timeline; andStrong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. 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. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Cincinnati PerksCincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageFlexible work scheduleCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with local nonprofit organizationsDiscounts on local sports games, fitness gyms and attractionsModern, ecofriendly campus with an on-site fitness centerStructured career paths with opportunities for professional growthDiscounted tuition for UC online programsAwardsNamed 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 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets
Job Locations
United States-OH-Cincinnati | United States | United States-TX-Irving (Dallas) | United States-CO-Denver
Category
Clinical Trial Management
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. We have just expanded our campus in Cincinnati and have offices in Dallas and Denver, and provide remote flexibility with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.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; andManage site quality, including direct supervision of project Clinical Research Associates 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-
required for home-based;Management of overall project timeline; andStrong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. 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. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Cincinnati PerksCincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageFlexible work scheduleCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with local nonprofit organizationsDiscounts on local sports games, fitness gyms and attractionsModern, ecofriendly campus with an on-site fitness centerStructured career paths with opportunities for professional growthDiscounted tuition for UC online programsAwardsNamed 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 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets