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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 Statistical Programmer
Job ID R0000034148 Newton, MassachusettsName of Employer: Parexel International LLC
Position Title: Principal Statistical Programmer
Position Location: 275 Grove Street, Newton, MA 02466
Hours: Full Time / 40 hours
Summary of Duties: Provide technical support and expert advice to internal and external sponsors on statistical programming projects to support clinical trial activities. Work independently to support various programming activities related to analysis and reporting of clinical study data. Fill the Statistical Programming Lead role on projects and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas. Monitor quality, timelines, resource allocation, and productivity in relation to budget. Project management for statistical programming. Advise and negotiate statistical programming timelines.
Education requirements: Bachelor’s degree in Statistics, Mathematics, Pharmaceutical Science, Data Analytics or related field of study. Employer will accept post-secondary academic coursework and/or relevant work experience which is evaluated as equivalent to a U.S. Bachelor’s degree in accordance with 8 CFR §214.2(h)(4)(iii)(D).
Experience requirements: 7 years of progressive experience in statistical programming.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
1) Programming and reporting process.
2) FDA 21 CFR Part 11 regulations;
3) ICH-GCP, CDISC, and WSOP guidelines;
4) Analyzing data from Phase I, II, and III clinical trials;
5) SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS Data Step, Proc Step, and Functions;
6) Generating reports, tables, and listings for statisticians;
7) Building structured, CDISC, SDTM or ADaM databases for clinical studies; and
8) Leading teams in a statistical programming environment.
*100% Remote reporting to Newton, MA.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #LV0209 to openings@parexel.com.
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