Senior Statistical Programmer Consultant

TL;DR

Senior Statistical Programmer Consultant (SAS/R): Supporting statistical programming for clinical trials and electronic submissions with an accent on CDISC standards, dataset validation, and data integration. Focus on collaborating with cross-functional R&D teams, managing CRO deliverables, and implementing technical guidelines to ensure high-quality clinical data outputs.

Location: Must be based in NJ, PA, or DE; Hybrid role

Company

hirify.global is a global full-service contract research organization (CRO) specializing in clinical development and functional solutions for the pharmaceutical and medical device industries.

What you will do

• Program and validate derived datasets, tables, figures, and listings for clinical trials.
• Ensure CDISC-compliant delivery for electronic submissions.
• Perform ad hoc exploratory analyses for clinical publications.
• Oversee programming deliverables from external CRO partners.
• Contribute to the design and implementation of SDTM/ADaM specifications and statistical analysis plans.
• Participate in the development of departmental guidelines and internal programming utilities.

Requirements

• Must reside in or be able to work from New Jersey, Pennsylvania, or Delaware.
• BS with 5+ years or MS with 3+ years of experience in statistical programming within the pharmaceutical industry.
• Proficiency in SAS and SAS Macro language.
• Working knowledge of R programming applied to clinical trials.
• Strong understanding of industry standards, GCP, 21 CFR, and ICH guidance.
• Experience with data integrations such as ISS and ISE.

Culture & Benefits

• Professional development focus with structured training programs.
• Opportunity to work directly for a single client while maintaining CRO career security.
• Supportive, diverse, and inclusive team environment.
• Industry-leading employee retention rates.

Hiring process

• CV screening.
• Phone interview as the initial evaluation step.