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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Senior Statistical Programmer - PRO
Job ID R0000033965 , IndiaThis 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
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