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.
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
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What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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