Medpace
Director, Clinical Trial Management (Incentives Available)
Medpace, Denver, Colorado, United States, 80285
Director, Clinical Trial Management (Incentives Available)
Job Locations:
United States-OH-Cincinnati | 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 senior-level Directors and established Project Managers to join our Clinical Trial Management Group in
Cincinnati, OH, Dallas, TX, Denver, CO or remotely with relevant experience.
Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. 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.
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.
Strong 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?
Hybrid work-from-home options (dependent upon position and level).
Competitive PTO packages, starting at 20+ days.
Competitive compensation and benefits package.
Flexible work schedule.
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, eco-friendly 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.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr
Job Locations:
United States-OH-Cincinnati | 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 senior-level Directors and established Project Managers to join our Clinical Trial Management Group in
Cincinnati, OH, Dallas, TX, Denver, CO or remotely with relevant experience.
Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. 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.
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.
Strong 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?
Hybrid work-from-home options (dependent upon position and level).
Competitive PTO packages, starting at 20+ days.
Competitive compensation and benefits package.
Flexible work schedule.
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, eco-friendly 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.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr