Medpace, Inc

Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more.. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance.. 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.. Discounts on local sports games, fitness gyms and attractions. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

management

Job Summary Medpace is continuing to add Sr. level Directors and experienced Project Managers to join our Clinical Trial Management Group in our newly established office in Denver, CO. This position will be responsible for mentoring CTMs as well as overseeing projects and sponsor relationships. Our therapeutic areas of focus include Oncology, 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. This position is a full-time office-based role in our Denver, CO office, with work-from-home flexibility following tenure with the company. Responsibilities <ul><li>Mentor Clinical Trial Managers, Project Coordinators, and other study team members in the Denver, CO office</li><li>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</li><li>Serve as primary Sponsor contact for operational project-specific issues and study deliverables</li><li>Maintain in depth knowledge of protocol, therapeutic area, and indication</li><li>Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided</li><li>Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable</li><li>Develop operational project plans</li><li>Manage risk assessment and execution</li><li>Manage study vendors where applicable</li><li>Manage site quality and monitoring deliverables</li><li>Work collaboratively with HR to support recruitment of new staff in Denver office</li><li>Serve as an escalation point for Clinical Operations in the Denver office</li><li>Implement and support Medpace corporate strategies in Denver office</li><li>Organize a cross-functional leadership team to align and support all associates in the Denver office. </li></ul>Qualifications <ul><li>Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred</li><li>Experience in Phases 1-4; Phases 2-3 preferred</li><li>5+ years as a project/clinical trial manager within a CRO</li><li>Management of overall project timeline</li><li>Bid defense experience</li><li>Strong leadership skills </li></ul>Compensation A target salary range of $175,000 - $250,000. Your compensation will be based on your skills and years of relevant experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter. 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. Denver Perks <ul><li>Denver Office Overview</li><li>Hybrid work-from-home options (dependent upon position and level)</li><li>Competitive PTO packages, starting at 20+ days</li><li>Competitive compensation and benefits package</li><li>Flexible work schedule</li><li>Company-sponsored employee appreciation events</li><li>Employee health and wellness initiatives</li><li>Community involvement with local nonprofit organizations</li><li>Structured career paths with opportunities for professional growth</li><li>Discounts on local sports games, fitness gyms and attractions</li><li>Modern, ecofriendly campus with an on-site fitness center</li><li>RTD Eco Pass</li><li>Secure bike storage room </li></ul>Awards <ul><li>Named a Top Workplace in 2024 by The Cincinnati Enquirer</li><li>Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility </li></ul>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

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