Senior Statistical Programmer

🕒 September 2

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $90k - $140k / year

⏰ Full Time

🟠 Senior

🖥 Software Engineer

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Everest Clinical Research

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2004

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.

📋 Description

• Design and specify study data tabulation models and analysis data models for clinical trials or integration of data from multiple trials, including ISS and ISE datasets • Generate complete and efficient analysis data models following approved dataset designs or specifications • Independently validate datasets created by other programmers or statisticians • Develop SAS programming codes and generate complete and accurate statistical output reports of trial data • Independently validate statistical output reports generated by other programmers or statisticians • Develop and test SAS codes for clinical trial database logical checks and reports for ongoing data review • Document data and programming information in accordance with corporate SOPs and guidelines • Archive clinical trial data and programming information in accordance with corporate archival SOPs and guidelines • Develop and provide expertise in other programming and system administration areas when required • Provide technical guidance and support to less experienced Statistical Programmers • Contribute to continuous improvement of statistical programming processes and procedures • Contribute to therapeutic area programming standards, conventions, and procedures as a lead programmer • Contribute to client-specific programming standards, conventions, and procedures when required

🎯 Requirements

• A Master’s in Math/Statistics • At least five years experience • Experience designing and specifying study data tabulation models and analysis data models for clinical trials or integrating clinical trial data from multiple trials • Knowledge of common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor’s requirements • Ability to generate analysis data models following approved dataset designs or specifications • Ability to perform independent validation of datasets and statistical output reports • SAS programming expertise • Ability to develop and test SAS codes for clinical trial database logical checks and reports • Knowledge of corporate SOPs, guidelines, and archival SOPs • Ability to provide technical guidance to less experienced Statistical Programmers

🏖️ Benefits

• Medical coverage • Dental coverage • Vision coverage • Life and AD&D insurance • Short-term disability • Long-term disability • Tuition reimbursement • Fitness reimbursement • Employee assistance program (EAP) • 401(k) retirement plan • Generous paid time off • Sick leave • Opportunity to earn a performance based bonus