Statistical Programmer II - PRO
India, Remote Job ID R0000033964 Category Statistical Programming Date Posted 06/06/2025Overview
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
This role supports the generation of evidence from patient-reported outcomes across multiple therapeutic areas, with a strong emphasis on oncology. The ideal candidate will have hands-on experience with clinical trial data, deep familiarity with PRO instruments, and strong SAS programming skills. Knowledge of CDARS and experience working in a global, cross-functional environment are essential.
Key Responsibilities
- Develop, validate, and maintain SAS programs for PRO data analysis, including derivation of endpoints, generation of TLFs, and QC of outputs
- Collaborate with statisticians, study leads, and cross-functional teams to interpret protocols and SAPs, define specifications, and deliver high-quality outputs
- Support the development and maintenance of standard templates and macros for common PRO instruments (e.g., EQ-5D, EORTC QLQ-C30, FACT-G)
- Participate in the creation and refinement of guidance documents, SOPs, and training materials for PRO programming workflows
- Ensure compliance with internal quality standards and regulatory expectations, including documentation of programming logic and QC processes
- Engage in biweekly PRO team meetings to share updates, troubleshoot issues, and align on priorities
Required Qualifications
- Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field
- 3–5 years of experience in statistical programming with a focus on clinical trial data and PRO endpoints
- Proficiency in SAS; working knowledge of R is a plus
- Strong understanding of CDARS and familiarity with CDISC standards
- Experience with multiple therapeutic areas; oncology experience is highly preferred
- Ability to work independently and collaboratively across time zones in a multicultural environment
Preferred Qualifications
- Familiarity with regulatory guidance on PROs and clinical outcome assessments
- Experience with automation tools and version control systems (e.g., Git)
- Exposure to project management tools like Monday.com
#LI-REMOTE
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
