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Advanced Clinical Trial Data Analyst
3 weeks ago
We're seeking a highly skilled Statistical Programmer to join our team. In this role, you'll have the opportunity to work on a variety of clinical trials, leveraging your advanced SAS programming skills and proficiency in CDISC standards.
As a Senior Statistical Programmer, you'll be responsible for performing data manipulation, analysis, and reporting of clinical trial data. You'll also generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures. Additionally, you'll create and review submission documents and eCRTs, and communicate with internal cross-functional teams and clients.
To be successful in this position, you'll need to have a strong understanding of SAS programming, CDISC standards, and clinical trial data. You should also have experience working with large datasets and be proficient in Efficacy analysis. We're looking for someone who is a team player, adaptable, and flexible when priorities change.
Here are the key qualifications we're looking for:
- Bachelor's degree in Statistics, Computer Science, Mathematics, or a related field
- At least 7 years of SAS programming experience in the Pharmaceutical & Biotech industry
- Strong knowledge of CDISC standards, including SDTM and ADaM
- Experience with clinical trial data, including safety and efficacy data
- Ability to work independently and as part of a team
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you're a motivated and detail-oriented individual with a passion for statistical programming, we encourage you to apply.