
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.
🕒 July 15
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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.
• Design and specify study data tabulation models and analysis data models for clinical trials or for the integration of clinical trial data from multiple trials • Generate complete and efficient analysis data models following approved dataset designs or specifications • Perform independent validation of datasets created by other programmers or statisticians • Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats • Develop SAS programming codes to independently validate statistical output reports of trial data 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 • Provide technical guidance and support to less experienced Statistical Programmers • Contribute to the continuous improvement of the statistical programming processes and procedures • Contribute to the establishment of therapeutic area programming standards/conventions/procedures within assigned therapeutic areas as a lead programmer • Contribute to the establishment of client specific programming standards/conventions/procedures for assigned clients when required
• A Master’s in Math/Statistics with at least five years experience
• upholding the principles of dignity, independence, integration, and equal opportunity • accommodations for candidates participating in any part of our recruitment and selection process
Apply Now🕒 July 14
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