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.
Key Responsibilities
- Develop and maintain global R codebase for generating CDISC ADaM datasets and tables, listings, and figures in accordance with clinical trial data requirements
- Ensure compliance with industry standards and regulatory requirements
- Collaborate with cross-functional teams to understand and implement project-specific data needs
- Provide technical expertise and support for data analysis and reporting tasks
- Perform quality control and validation of outputs to ensure accuracy and consistency
- Contribute to process improvements and development of programming standards using R
Qualifications
- Bachelor's degree in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Data Science)
- Minimum of 3 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival)
- Familiarity with data visualization techniques and tools in R
- Experience with clinical trial data and familiarity with CDISC ADaM and SDTM standards
- Knowledge in Industry R packages like ADMIRAL and OAK
- Strong analytical and problem-solving skills
- Excellent communication and teamwork abilities
Desirable Skills
- Knowledge of other open-source packages and tools
- Experience with SAS software
- Familiarity with CRAN, POSIT, and other open-source repositories and products
Top Skills
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.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:
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sexual preference or orientation, nationality or political beliefs.
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• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
