Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team!Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Medical Writer to join our Regulatory Affairs team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.Write clinical study reports, protocols, clinical development plans, FDA briefing documents, and IND, NDA, and MAA modules;Coordinate quality control reviews of documents and maintaining audit trails of changes; andProvide input on data analysis planning and interpretation.QUALIFICATIONSDegree in a life science or engineering field (PhD preferred);Prior experience in the research, pharmaceutical, or medical device industry preferred;Strong computer skills, project management skills, and a high attention to detail; andStrong communication skills (both written and oral).WHY MEDPACE?At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.AWARDSMedpace is being recognized locally, nationally, and globally for their work in the industry as well as the culture they have developed for their team.Medpace Named a Top Cincinnati Workplace for 2015, 2016 and 2017 by the Cincinnati EnquirerMedpace named Top Ten CRO in 2015 CenterWatch Investigative Site SurveyEagle Award winner and nominee - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships.WHAT TO EXPECT NEXTWe look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.EO/AA Employer M/F/Disability/Vets
Website : http://www.medpace.com
A global leader in research-based drug and medical device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval. As a therapeutically-focused Contract Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.