Associate Director – Study Start-Up (Regulatory Submissions) Job Locations United States-OH-Cincinnati Category Clinical Operations Overview Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 3,000 people across 36 countries. Responsibilities We are seeking a key associate director to support the Medpace Regulatory Submissions, Study Start-Up team in the US.
This position will be an integral part of the Medpace clinical operations management team. This role will be responsible for the strategic development of the group, management of the team, and continuous improvement of processes. As a leader of the Regulatory Submissions team you will be responsible for providing input on new business development opportunities, developing and maintaining relationships with clients, and providing guidance and support in regards to study start-up. A general understanding of study start-up and how the role of regulatory submissions is integrated with other clinical operations functions is preferred.
- BA/BS degree in Life Sciences or related field, or equivalent combination of education and experience. Advanced degree, preferred
- High level of study start-up experience within a contract research organization or pharmaceutical company
- Excellent presentation, negotiation, documentation, and leadership skills, as well as strong team-orientation and interpersonal skills
- Excellent written/oral communication and organization skills; Customer focus with the ability to manage challenging priorities and remain flexible and adaptive in stressful situations; and, Experience managing a group.
Why Medpace? When you join Medpace, you become part of a team dedicated to supporting the development of groundbreaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying competitive total compensation and benefits package and internal growth opportunities. Awards Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer Winner of the ACRP-Avoca CRO Quality Award in 2018 Recognized with six CRO Leadership Awards from Life Science Leader magazine Eagle Award winner – which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships What to Expect Next We look forward to receiving your application. A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview. EO/AA Employer M/F/Disability/Vets
Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process. Options Apply for this job online Apply Share Email this job to a friend Refer Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed Need help finding the right job? We can recommend jobs specifically for you! Click here to get started. Application FAQs Software Powered by iCIMS www.icims.com