AxiStat, Inc.
Statistician
Key Responsibilities:
Assists senior statistician on statistical and programming activities for pre-clinical, Phase 1, 2, 3 and/or Phase 4 clinical trials and epidemiologic studies. Specific responsibilities include:
o Collaborate with Data Management and review Case Report Forms, completion guidelines, edit check specifications
o Write detailed Statistical Analysis Plans incorporating appropriate statistical methodology for analysis of clinical trial and epidemiologic data, and develop mock tables and listings
o Work with the SAS programmers on development of analysis database specifications and programming of tables, listings and figures
o Complete program validation and quality control of tables, listings and figures produced by the SAS programmers
o Review randomization schedules and implementation procedures
Assist SAS programmers in testing of SAS macro library for statistical programming
Participate in internal study team meetings
Qualifications and Abilities:
M.S. in biostatistics, statistics, epidemiology or other relevant scientific discipline
At least 2 years experience in the pharmaceutical/biotech industry at either a contract research organization or pharmaceutical/biotech company, or equivalent relevant clinical study experience
Knowledge of statistical methods for clinical studies
Knowledge of SAS and other statistical programming packages
Excellent oral and written communication skills
Ability to work in a collaborative and multi-disciplinary environment
Please send resumes to statjobs@axistat.com.
Statistical Programmer I
Key Responsibilities:
Develop, test and validate SAS programming code for analysis databases, tables, listings and figures
Write SAS programs for validation and quality control of analysis databases, tables, listings and figures
Program SAS edit checks and validation programs to assist with data management activities
Assist Statisticians with developing and maintaining analysis database specifications
Assist Statistical Programmer II with testing and maintaining SAS Macro library
Write SAS programs for database integration and submission of data to regulatory agencies, including data in CDISC format
Ensure adherence to quality control procedures for statistical programming activities
Participate in internal study team meetings
Qualifications and Abilities:
B.S. or B.A. in computer science, statistics, or other relevant scientific discipline
At least 2 years experience SAS programming with a minimum of one year programming using clinical study data in either a contract research organization or pharmaceutical/biotech company
Excellent knowledge of SAS Base and SAS Stat. Experience with SAS Macro and SAS Graph preferred.
Excellent oral and written communication skills
Ability to work in a collaborative and multi-disciplinary environment
Please send resumes to careers@axistat.com.
*No Visa Sponsorships/Transfers available.
*Position is Full-Time only
*Minimum of 2 years of Statistician/Statistical programming experience in Biotech / Pharmaceutical / Device or CRO environment MUST be within the US.
*No Relocation Allowance
Posted 1/17/2012