Medpace
Director - Study Start-Up Project Management (Incentives Available)
Medpace, Denver, Colorado, United States, 80285
Director - Study Start-Up Project Management (Incentives Available)
Job Locations:United States-OH-Cincinnati | United States-CO-Denver | United States-TX-Irving (Dallas)Category:
Site Activation & MaintenanceJob Summary
We are seeking an office based
Director of Study Start-Up
to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations Senior Management team. A strong understanding of study start-up and how the role of regulatory submissions is integrated with other clinical operations functions is preferred.Incentives can include:
Competitive bonus program, sign-on/relocation bonus, and equity awards.Location:
Position can be office based in Cincinnati, Dallas or Denver.Responsibilities
Contribute directly to the growth and strategic development of a large, global Study Start-Up team;Develop and identify continuous improvement opportunities of internal processes;Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;Provide input on new business development opportunities;Develop and maintain relationships with clients.Qualifications
Bachelor's degree in Life Sciences or related field; Advanced degree is preferred;8+ years as a study start-up senior leader within a CRO;Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;Excellent written and oral communication;Experience managing and developing a team.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 Perks:Hybrid 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 programsAwards
Named a Top Workplace in 2024 by The Cincinnati EnquirerRecognized 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 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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Job Locations:United States-OH-Cincinnati | United States-CO-Denver | United States-TX-Irving (Dallas)Category:
Site Activation & MaintenanceJob Summary
We are seeking an office based
Director of Study Start-Up
to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations Senior Management team. A strong understanding of study start-up and how the role of regulatory submissions is integrated with other clinical operations functions is preferred.Incentives can include:
Competitive bonus program, sign-on/relocation bonus, and equity awards.Location:
Position can be office based in Cincinnati, Dallas or Denver.Responsibilities
Contribute directly to the growth and strategic development of a large, global Study Start-Up team;Develop and identify continuous improvement opportunities of internal processes;Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;Provide input on new business development opportunities;Develop and maintain relationships with clients.Qualifications
Bachelor's degree in Life Sciences or related field; Advanced degree is preferred;8+ years as a study start-up senior leader within a CRO;Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;Excellent written and oral communication;Experience managing and developing a team.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 Perks:Hybrid 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 programsAwards
Named a Top Workplace in 2024 by The Cincinnati EnquirerRecognized 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 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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