Mid-Level Biostatistician. Newton LilyLifestyle

Aligning values for better health outcomes.

At Parexel, our shared mission is to enhance global health. We provide comprehensive clinical development solutions ranging from clinical trials to regulatory consulting and market access, all driven by our deep conviction in our work.

Every team member plays an essential role in developing therapies that will benefit patients. Our work is personal, empathetic, and dedicated to making a significant difference.

275 Grove Street, Suite 101C, Newton, MA 02466. Telecommuting is permitted from anywhere in the US up to 5 days per week.

Parexel International LLC is seeking a Mid-Level Biostatistician to conduct statistical analyses for clinical trials, ensuring compliance with industry standards and regulations under minimal supervision.

Responsibilities include:

• Completing statistical analysis projects on time and within budget, in collaboration with cross-functional teams.
• Performing quality control of datasets, tables, figures, and data listings produced by colleagues.
• Applying advanced statistical methods accurately and efficiently.
• Defining randomization procedures and authoring the statistical sections of protocols and analysis plans.
• Acting as the primary liaison for clients regarding statistical and contractual matters.
• Providing training on statistical analysis techniques to internal stakeholders.
• Producing and quality-checking both basic and advanced statistical outputs using effective programming techniques.
• Participating in client meetings to present analysis concepts and discuss results.

The annual salary for this position is between $ and $139,300.

• Master's degree in Biostatistics or a relevant field, with at least 6 months of statistical analysis experience.
• 6 months of proficiency in programming with SAS, R, Python, and MATLAB.
• Experience leading statistical projects in biomedical research across multiple therapeutic areas.
• Skills in analysis and statistical modeling, including ANCOVA, logistic regression, survival analysis, and MMRM.
• Familiarity with statistical analyses in both early- and late-phase clinical trials and drug development.
• Ability to create table, listing, and figure shells.
• Experience with FDA/CDISC standards.
• Proficiency in reviewing SDTM and ADaM datasets as well as table, listing, and figure outputs.

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, including race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.