Job Description
Overview
We are seeking a Senior Statistical Programmer to provide programming support for clinical studies and regulatory submissions. This role involves developing, validating, and maintaining CDISC-compliant datasets and outputs to support data analysis and reporting activities.
Key Responsibilities
- Develop and validate CDISC-compliant SDTM and ADaM datasets in support of clinical studies and submissions.
- Create and maintain programs to generate tables, figures, and listings (TFLs) for ad-hoc analyses and publications.
- Draft and maintain dataset specifications in accordance with SDTM IG, ADaM IG, and SAP.
- Develop and optimize SAS macros and utility programs to streamline processes.
- Design, test, and implement programming solutions to meet complex project needs.
- Collaborate effectively with cross-functional teams while managing multiple projects and deadlines.
Qualifications
- Bachelor’s degree in Mathematics, Statistics, Computer Science , or a related field.
- Advanced SAS programming skills required.
- CDISC SDTM/ADaM experience required; submission experience strongly preferred.
- Strong verbal and written communication skills.
- Experience with additional statistical software (e.g., R, S-Plus, WinBUGS ) a plus.
- Programming experience with VBA, C++, or Python beneficial.
- Previous experience in pharmaceutical or biotechnology industry preferred.
Why Apply
This is an excellent opportunity to leverage your programming expertise in a collaborative, data-driven environment. If you’re ready to contribute to impactful clinical research projects, we’d love to hear from you.
Apply today to learn more!
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