Senior Statistical Programmer

Job Responsibilities:

• Provide statistical programming support for data analyses on Preclinical/clinical/post marketing studies.
• Develop CDISC SDTM and ADaM datasets, and DEFINE.XML.
• Program and validate SAS programs to produce summary tables, listings, and figures for clinical study reports.
• Review key study-related documents, such as Protocol, SAP, CRFs, Data Management Plan, Data Transfer Specifications, and other related documents.

Desired skills:

Senior Statistical Programmer typically requires at least 5 years of industry experience supporting clinical trials in the Pharmaceutical industry with either a BS or MS degree in Biostatistics, Computer Sciences, or equivalent. Strong Base SAS, SAS/STAT, SAS/GRAPH, SAS Macro, and SAS ODS are expected.

Statistical Programmer I

• Statistical Programmer I typically requires at least 2 years of industry experience of using SAS with either a BS or MS degree in Biostatistics, Computer Sciences, or equivalent.
• HCV, HIV, Oncology experience is a plus.

To apply:

Please email your resume to jobs@clinbiometrics.com

Senior/Principal Statistical Programmer

Job Responsibilities:

• Provide statistical programming support for Phase I to Phase III clinical studies
• May participate in NDA filing and related activities
• Program and validate analysis datasets (SDTM, ADaM), tables, figures and listings
• Create programming specification
• Comply with Company SOPs and ensure programming documentation is completed according to SOPs

Desired skills:

• Minimum of 5 years of SAS programming experience, including 3 years in pharmaceutical setting
• Working knowledge and implementation experience with SDTM and ADaM standards
• Prior experience working in the therapeutic areas of Oncology, Virology, Cardiovascular or Inflammation
• Prior experience with NDA filing
• Ability to work effectively with minimum supervision
• Excellent verbal and written communication skills

To apply:

Please email your resume to jobs@clinbiometrics.com