When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job 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: Masters 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. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the worlds life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcares most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients With Heart.
