#977 - Statistical Programmer II

Job Opportunity only available for professionals located in Latin America.

We're seeking an experienced Statistical Programmer II to support clinical development programs within the Biometrics organization. This role is intended for a programmer with 2–3 years of pharmaceutical industry experience who can independently deliver high-quality, compliant, and submission-ready statistical programming deliverables across clinical trials.
The Statistical Programmer II will work closely with biostatisticians, data management, and cross-functional partners to ensure accurate implementation of analysis specifications and regulatory standards, contributing directly to clinical trial analyses, regulatory submissions, and inspection readiness.

Requirements:

• Advanced English level (B2/C1/C2) to ensure fluent communication with customers and teams.
• 2–3 years of statistical programming experience within a pharmaceutical, biotechnology, or clinical research organization.
• Strong hands-on experience with SAS for clinical trial programming; working knowledge of R preferred.
• Solid understanding of clinical trial data structures and end-to-end development processes.
• Working knowledge of CDISC standards, including ADaM; familiarity with SDTM required.
• Understanding of regulatory expectations for statistical programming, including documentation, traceability, and inspection readiness.
• Demonstrated ability to manage multiple deliverables independently while meeting timelines and quality expectations.
• Strong analytical, problem-solving, and troubleshooting skills.
• Effective written and verbal communication skills, with the ability to collaborate across cross-functional teams.
• High attention to detail, strong documentation practices, and commitment to quality and compliance.

Responsibilities:

• Independently develop, validate, and maintain analysis-ready datasets in accordance with approved specifications, including:
• ADaM datasets
• Supporting analysis datasets required by the SAP
• Program, generate, and validate Tables, Listings, and Figures (TLFs) using SAS, ensuring alignment with approved SAPs, shells, and programming standards
• Perform independent QC and peer review of datasets and outputs to ensure accuracy, traceability, and reproducibility
• Implement and enforce CDISC standards, including SDTM (as applicable) and ADaM, across assigned studies
• Collaborate closely with Biostatistics to translate SAP requirements into robust and efficient programming solutions
• Partner with Data Management to resolve data issues and ensure consistency between SDTM and ADaM datasets
• Support ongoing data review, including identification of data trends, anomalies, and potential risks to analysis integrity
• Ensure all programming deliverables are submission-ready and inspection-ready, in compliance with internal SOPs and global regulatory expectations
• Support preparation and delivery of programming components for regulatory submissions (e.g., NDA, BLA, MAA)
• Maintain complete and compliant programming documentation, including specifications, program headers, and QC records
• Contribute to the development and optimization of programming standards, macros, and reusable code
• May provide informal guidance or technical support to junior statistical programmers

What do we offer?

• 100% Remote work.
• Competitive salary in USD.
• Type of contract: Independent Contractor with Venon Solutions LLC.
• Contract duration: Long-term.
• 2 weeks of PTO (paid time off).
  
• Paid Holidays: from the Client's calendar (USA)
• Working hours: Full-time EST timezone, fully committed.