Job Description
Cytel Inc. (Cambridge, MA) is seeking Senior Statistical Programmers to work directly with stakeholders to lead and contribute to statistical programming projects and to ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements. Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results. Provide relevant training and mentorship to staff and project teams on SAS techniques and clinical trial data with respect to CDISC standards and other regulatory requirements. 100% telecommuting.
Minimum Requirements: Bachelor's degree in Statistics, Health Informatics, Biochemistry, or a closely related field and 6 years of experience in biostatistics or statistical programming activities in the Pharmaceutical or Biotechnology industry in clinical development, including: 2 years of experience in SAS programming; 2 years of experience with CDISC ADaM and SDTM, ICH Statistical, and Clinical Report guidelines; and 1 year of experience as lead statistical programmer working with global cross functional teams to include project management.
Will also accept a Master's degree in Statistics, Health Informatics, Biochemistry, or a closely related field and 3 years of experience in biostatistics or statistical programming activities in the Pharmaceutical or Biotechnology industry in clinical development, including: 2 years of experience in SAS programming; 2 years of experience with CDISC ADaM and SDTM, ICH Statistical, and Clinical Report guidelines; and 1 year of experience as lead statistical programmer working with global cross functional teams to include project management. To apply, contact jayne.stegman@cytel.com with job ID 724 in subject line.