Director, Clinical Trial Management NASH (Incentives Available)
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Mon, 26 Apr 2021 23:59:59 GMT
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Director, Clinical Trial Management – NASH (Incentives Available) Job Locations United States-OH-Cincinnati Category Clinical Operations 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 approximately 3,500 people across almost 40 countries. 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. Therapeutic area of focus is NASH and more. We provide remote flexibility with relevant experience. 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 – Responsible for management of study vendor – Manage site quality, including direct supervision of project Clinical Research Associates 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 Why Medpace? When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking 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 a competitive total compensation and benefits package and internal growth opportunities. Awards: – Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer – Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability – Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next: 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 *WARNING: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.