Director - Study Start-Up Project Management (Incentives Available)
Medpace
Overview 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 leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required. 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; and 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; and 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 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. #J-18808-Ljbffr Medpace
$82.5k - $103k
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...As a Health & Benefits Consultant, Project Manager , you will assist with managing consulting... ...placement, benchmarking, and other studies. Develop sophisticated benefits design... ...may be eligible for performance-based incentives. We are excited to offer a competitive...Minimum wageWork at officeLocal areaRemote workFlexible hours3 days per week1 day per week- ...time,office-basedAssociate Clinical Trial Manager (aCTM) position in our Cincinnati, OH... ...Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers... ...ResponsibilitiesCommunicate and collaborate on global study activities; working closely with the...Full timeContract workWork at officeWork from home
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- ...information, visit Job Summary The Associate Director, Site Budgets provides leadership in the development, management and oversight of the trial site budgets... ...standards and business requirements across studies and projects. Proactively identify risks, capacity constraints...Contract work
$100k - $115k
...one of our flagship clients, while also managing a portfolio of additional retainer accounts... ...is a remote role that requires on-site availability in Cincinnati once per week. This... ...be willing to travel on occasion when a project or company initiative requires their attendance...Full timeTemporary workLive inRemote workFlexible hoursShift work1 day per week$153k - $297k
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$70k - $140k
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$124k - $280k
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