Senior Biostatistician

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 may telecommute from anywhere in the U.S. up to 5 days per week.

Job Title: Senior Biostatistician

Job Duties: Parexel International LLC seeks a Senior Biostatistician based in Newton, MA, to work independently in the production and quality control of analysis plans, reports, derived datasets, tables, listings and figures, provide statistical advice to clients and fulfil the project primary role within a designated project team. Coordinate and lead project team to successful completion of a project within given timelines and budget. Serve as key contact for clients’ statistical and contractual issues. Produce analysis plans, statistical reports, statistical sections of integrated clinical reports, and other process supporting documents. Provide training in statistical analysis to internal clients. Lead data review meetings and SAP kick-off meetings. Proactively participate in and lead process and quality improvement initiatives. Discuss analysis concepts and present and discuss study results with clients. Mentor and train more junior members of the department. Prepare for and attend bid defense meetings to support business development. Position may telecommute from anywhere in the U.S. up to 5 days per week.

Minimum Requirements: Employer requires a Master’s degree in Biostatistics, Statistics, or a related field, plus 1 year of statistical analysis experience in: 1) Clinical data structure and process; 2) Generating clinical outputs from EDC data; 3) Statistical analysis in a clinically related subject, within clinical trials; 4) Programming with SAS and R; 5) Developing randomization specification and generating randomization list; 6) Developing statistical analysis plans and Mock Shells for tables, figures, and listings (TFLs); and 7) Reviewing TFLs, statistical analysis reports, and ADaM data specification.

To apply, please send resume to openings@parexel.com and cite requisition number 00927, 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.