Senior Statistical Programmer #3470594

Axiom Path; United States; On-site; USD 80,000 - 100,000; Full time

Job summary

A leading biopharmaceutical organization in the United States is seeking a Recruitment Administrator/Technical Recruiter/Credentialing Specialist. The role involves providing programming support for clinical trials and developing datasets aligned with CDISC standards. The ideal candidate has over 5 years of SAS programming experience and must be detail-oriented with strong communication skills. This position offers professional growth in a collaborative environment.

Qualifications

• Minimum of 5 years of SAS programming experience in the pharmaceutical or biotechnology industry.
• Proven expertise in CDISC standards (SDTM and ADaM).
• Experience supporting data for regulatory submissions (e.g., FDA, EMA).

Responsibilities

• Provide programming support for clinical trials and regulatory submissions.
• Develop and validate SDTM and ADaM datasets aligned with CDISC standards.
• Generate high-quality tables, figures, and listings for studies and publications.

Skills

SAS programming expertise

Attention to detail

Communication skills

Organizational skills

Education

Bachelor's degree in Mathematics, Statistics, Computer Science, or related field

Master's degree (preferred)

Tools

SAS

R

Python

VBA

Job description

Recruitment Administrator/Technical Recruiter/Credentialing Specialist/Customer service/Data Entry Specialist

Be Part of a Dynamic Biostatistics & Biometrics Team

This leading biopharmaceutical organization is advancing treatments for complex and rare diseases through innovative science and data-driven excellence. The Biometrics department is known for its collaborative culture and analytical rigor, ensuring clinical data is transformed into meaningful insights that drive regulatory and clinical success. Team members operate in a high-performance environment that values innovation, precision, and partnership across global development programs.

What’s In Store For You

This contract opportunity, based in Bridgewater, NJ, offers the chance to work on cutting-edge statistical programming initiatives that support global clinical studies. The position provides exposure to regulatory submissions, cross-functional collaboration, and professional growth in a world-class biostatistics environment.

How You Will Make an Impact

• Provide programming support for clinical trials and regulatory submissions.
• Develop and validate SDTM and ADaM datasets aligned with CDISC standards.
• Generate high-quality tables, figures, and listings for studies and publications.
• Develop, maintain, and enhance SAS macros and utilities to optimize workflows.
• Collaborate with Biometrics and Biostatistics teams to ensure consistent deliverables.
• Uphold accuracy, efficiency, and compliance in all programming outputs.

Qualifications

• Bachelor’s degree in Mathematics, Statistics, Computer Science, or related field (Master’s preferred).
• Minimum of 5 years of SAS programming experience in the pharmaceutical or biotechnology industry.
• Proven expertise in CDISC standards (SDTM and ADaM).
• Experience supporting data for regulatory submissions (e.g., FDA, EMA).
• Familiarity with R, Python, or VBA a plus.
• Strong attention to detail, communication, and organization skills.

To apply, please submit your resume and cover letter highlighting your relevant experience and qualifications.

About Axiom Path

Axiom Path is a global solutions provider leveraging AI and pre-built analytics to deliver exceptional services across various domains. Our core values (Accountability, Excellence, Integrity, and Community) guide us in providing optimized results and unparalleled service. We are an equal opportunity employer, a SIA-recognized diversity-owned firm, committed to diversity and inclusion.