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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