Work Flexibility: Hybrid

What you will do

Generate statistical summary tables, patient data listings, and reports using SAS.Handle complex SAS programming issues , perform database and CRF review to ensure programming consistency, and be familiar with all study programming issues.Contribute to statistical analysis plans.Prepare template and programming for periodic progress reports for assigned clinical programs.Compile clinical data and relevant back-up material and present these results to the Biostatistics Manager for review.Work on SAS programs to generate data sets, tables, listings, and graphs.Work on SAS programs to complete quality control and validation work on SAS programs, data sets, and TLGs generated by others.Work on SAS programs to process and/or import external data into analysis data sets or export SAS output to other computer files for delivery.Work on SAS programs to create derived variables and data sets (e.g., LOCF (Last Observation Carry Forward), adverse events with multiple merging and cleaning procedures), or perform other required advanced data manipulation to support completion of biostatistics projects; SAS, SQL & Macro skills required.May be required to assist in other programming tasks using software other than SAS to support biostatistics or specialized data analysis requirements.Assist with documents to describe SAS programs as assigned, such as specifications for protocol analysis data sets.Perform group and departmental Quality Control (QC) procedures.Work on listings to support data cleaning and monitoring.

What You Need:

Required Qualifications:

Bachelor's Degree or equivalent in biostatistics, statistics, or related fieldThe ideal candidate will have at least 5-8 years of experience in SAS programming and analysis of clinical trial data.Familiarity with clinical trial design and analysis issues.Experienced with electronic data capture (EDC) system(s).

Preferred Qualifications:

Medical device experience

Travel Percentage: 10%