Jobs at Parexel
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.
Biostatistician II
Job ID R0000041671 Newton, MassachusettsJob Location: 275 Grove Street, Suite 101C, Newton, MA 02466 and telecommuting permitted from anywhere in the US up to 5 days per week.
Job Title: Biostatistician II
Duties: Parexel International LLC seeks a Biostatistician II based in Newton, MA to conduct statistical analysis on clinical trials according to industry standards and government regulations under limited supervision. Complete clinical trial statistical analysis projects within timeline and budget in coordination with cross-functional project teams. Perform QC of derived datasets, tables, figures, and data listings produced by other members of the department. Understand and apply advanced statistical methods. Responsible for defining the randomization specifications and writing statistical sections of protocols, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents. Liaise with clients as key contact with regard to statistical and contractual issues. Provide training in statistical analysis to internal clients. Conduct the production and QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques. Attend and actively contribute to client meetings as appropriate, including discussing and presenting analysis concepts and study results. Telecommuting permitted from anywhere in the US up to 5 days per week. (Ref. #: 00981). Annual salary: $106,400.28 - $139,300.
Requirements: Master’s degree in Biostatistics or a related field plus 6 months of statistical analysis experience. Must have 6 months of experience in each of the following: (1) Programming in SAS, R, Python, and MATLAB; (2) Leading projects in biomedical research, including leading the development and execution of statistical analysis plans in multiple therapeutic areas; (3) Analysis and statistical modelling utilizing ANCOVA, logistic regression, survival analysis, and MMRM; (4) Statistical analysis in early- and late-phase clinical trials and drug development; (5) Creating table, listing, and figure shells; (6) FDA/CDISC experience; and (7) Reviewing SDTM and ADaM datasets, and table, listing, and figure outputs.
To apply, please send resume to openings@parexel.com and cite requisition number 00981 or apply at jobs.parexel.com.
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs