Nashville Clinical Research Networking Event Job Locations United States-TN-Nashville 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. Job Summary
Networking Event on February 19th in Nashville, TNMore details regarding location and times will be given out once selected for event. Responsibilities Clinical Research Associate (CRA) Comprehensive training program that will provide you the resources and knowledge to monitor sites independently; Must be willing to travel 60-80%; Communicates with medical staff and clinical research physicians; and Work with world class research sites.
Regulatory Affairs Opportunities (including Regulatory Project Management, Medical Writing, and Regulatory Operations) Develop regulatory strategies to create state-of-the-art drug development plans; Regulatory project leadership to facilitate interactions between drug sponsors, health authorities, and subject matter experts to accelerate drug development; and Fast-paced team environment with the opportunity to work closely with all functional areas across the globe.
Project Coordinator (PC) Partner with Clinical Trial Manager to coordinate daily study activities Central point of contact for internal and external team members Create and maintain project timeline
Regulatory Submissions Coordinator (RSC) Assist with the start-up of clinical research sites Collaborate with Institutional Review Boards (IRBs) Prepare regulatory documents, including Informed Consent Forms
Regulatory Submission (Study Start-Up Manager) Efficiently manage and successfully execute all aspects of global start-up; Perform quality checks on submission documents and site essential documents; and Prepare and approve informed consent forms.
Clinical Trial Manager (CTM) Postdoctoral Research or Healthcare research experience required Management of project timelines and all project deliverables Responsible for leading internal project team members
Patient Recruitment Manager Sets and oversees the execution of recruitment/retention strategic plans for clinical trial recruitment. Manages overall trial strategy to continually improve and drive efficiencies throughout a campaign. Works withinternal and external teams to evaluate and integrate innovative technologies.
GCP QA AuditorCoordinate and conduct internal system audits and external investigative site/vendor audits in accordance with Good Clinical Practice (GCP) guidelines; Create, maintain, and revise departmental standard operating procedures, forms, and templates; Host audits by sponsors and regulatory inspectors; Coordinate, conduct, and track company-wide regulatory training (ICH/GCP and medical device); Develop training materials and applicable tests and guides; and Work with outside clients/sponsors. 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 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.
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*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. 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
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