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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Principal Biostatistician
Job ID R0000034224Provide broad statistical support for trial designs, protocols & CRF development on specific studies; Lead production & quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports & other process supporting documents; and Perform sample-size calculations, generate randomization lists & write statistical methodology sections for inclusion in study protocols.
Must have a Master's Degree in Medical Statistics or a related field, and 5 years of experience with each of the following:
(i) Leading interactions w/multidisciplinary study across different time-zones;
(ii) Contributing to planning & delivery of core documents, such as Clinical Study Report, Statistical Analysis Plan & publications;
(iii) Collaborating on SDTM & ADAM specifications & quality control;
(iv) Developing & QC SAS or R programs & across, tables, listings & figures as specified in the SAP; and
(v) Mentoring junior biostatisticians.
Experience may be gained concurrently. 100% Telecommuting permitted from within the United States. Pay rate: $165,000. Apply online at: https://jobs.parexel.com/en/search-jobs or by sending your resume to openings@parexel.com and reference: 000523
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