Description
Statistical ProgrammerThe main responsibilities of this role include, but are not limited to:
- Processes clinical data for analysis of clinical trials for Phase 1-4 in the Infectious Disease Therapeutic Area
- Programs study report tables, listings and figures as well as ad-hoc requests for publications, posters and other needs
- Provides programming and general support for Advisory Committee meetings
- Develops SAS coding and table templates for preparing, processing and analyzing clinical data
- Follows good programming practices; adequately documents programs while being compliant with ICH-GCG guidelines and company SOPs
- Generates and QC summary tables, data listings and graphs for in-house analyses of study data or publications using SAS standard coding practices
- Develops tools to improve programming efficiency or quality
- Creates and reviews programming plans and specifications for datasets and TLFs
TRAINING AND EDUCATION:
- A minimum of a Bachelor's degree in Computer Science, Mathematics, Statistics, Pharmaceuticals Sciences, Life Sciences and related areas is required; Master's degree is preferred
- SAS certification is a plus
PRIOR EXPERIENCE:
- A minimum of 5 years hands on career experience with SAS in the pharmaceutical or biotechnology industry
- Experience as a lead programmer for a study is preferred
- Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting
- Well versed with CDISC conventions, i.e., SDTM and ADaM models
- Very familiar with SAS Statistical Procedures
- Knowledge of applicable standards, regulations and ICH-GCP for clinical study conduct
- Excellent knowledge of SAS programming and associated features and their applications in pharmaceuticals industry environment in particular clinical trial data setting
To find out more about Real please visit www.realstaffing.com