I contribute to clinical research with expertise and empathy. And I do it
Statistical Programmer II
Primary Location: United States, Newton, Massachusetts Job ID R0000042117 Category Statistical Programmer Date Posted 05/26/2026Overview
As a member of Parexel’s Statistical Programming group, you analyze, summarize, and graphically present clinical data to assess the safety and efficacy of the clinical trial. It requires attention to detail, a commitment to quality, and effective communication to ensure new treatments reach patients faster. You will work in different therapeutic areas assessing a variety of data entries and endpoints in an ever-changing environment. We provide a fertile environment for growth, with extensive training, mentoring, and technical knowledge sharing.
You will work closely with the client and Parexel teams and collaborate to maximize the collective strength. Experience a supportive and motivating work environment where our teams offer an inherent breadth of knowledge within a diverse and inclusive workplace.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Analytical
- Detail-oriented
- Independent
- Proactive
- Responsible
- Team-player
About This Role
Job Location: 275 Grove Street, Suite 101C, Newton, MA 02466 and position may telecommute from anywhere in the United States 5 days per week.
Job Title: Statistical Programmer II
Duties: Parexel International LLC seeks a Statistical Programmer II reporting to headquarters in Newton, Massachusetts to conduct statistical programming. Use programming techniques to produce derived datasets (e.g., SDTM, ADaM), tables, figures, and data listings in compliance with CDISC standards. Provide technical expertise for clinical trials and support programming activities related to analysis and reporting of clinical study data. Assist in project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation. Create define.xml files and reviewer guides for inclusion in regulatory submissions. Use efficient programming techniques to quality control low-medium complexity derived datasets, tables, figures, and data listings. Produce Tables, Listings, and Figures (TLFs) for clinical study reports, regulatory submissions, and publications. Assist in the production and quality control of derived dataset specifications and other process supporting documents and submission documentation. Implement statistical analysis plans (SAPs) by writing SAS code. Provide training and mentorship to staff and project teams. Maintain all supporting documentation for studies in accordance with SOPs and guidelines to ensure traceability and regulatory compliance. Ensure compliance with SOPs, guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal and external audits and regulatory inspections. Participate in process/quality improvement initiatives and work with P21 Enterprise version. Position may telecommute from anywhere in the United States 5 days per week. Annual salary: $115,790.20 - $132,400.
Requirements: Bachelor’s degree in Statistical Programming, Mathematics, Statistics, Data Analytics, Business Administration, or a related field plus 5 progressive years of statistical programming experience. Must have five years of experience in each of the following: (1) Developing and validating SAS programs for clinical trial data analysis, including data cleaning, data integration, and report generation; (2) Creating and maintaining Analysis Data Model (ADaM) datasets in compliance with CDISC standards; (3) Producing Tables, Listings, and Figures (TLFs) for clinical study reports, regulatory submissions, and publications; (4) Implementing statistical analysis plans (SAPs) by writing SAS code; (5) Performing quality control checks on SAS programs and outputs produced by other team members; (6) Maintaining, and utilizing standard SAS macros and tools, including Base, Stat, Macro, EG, Studio, Graph, ODS, and Report; (7) Creating define.xml files and reviewer’s guides for inclusion in regulatory submissions; (8) Working with ICH-GCP and 21 CFR Part 11.
To apply, please send resume to openings@parexel.com and cite requisition number 00979 or apply at jobs.parexel.com. This position is subject to the company’s Employee Referral Program.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Potential Career Path
Parexel offers career paths for Statistical Programmers to progress in their technical position or managerial position, as well as options to move to other areas of the business.
- Statistical Programmer I
- Statistical Programmer II
- Senior Statistical Programmer
- Subject Matter ExpertPeople Management
Employee Insights
Why Statistical Programmers work at Parexel
