Qualified Applicants will possess:

Clinical Data Analyst/Programmer

Must have a Master's degree or equivalent in  computer science, engineering (any), molecular sciences, nanotechnology or related plus 2 years of experience in the job offered or related occupation as a computer software professional.                  

Analyze, design and develop programs to accomplish various processes of clinical trials.

Design and document databases for data entry and/or electronic data transfers to meet requirements of the analysis plan. 

Create data sets for data analysis end/or for transfer to external groups as necessary, including potential integration of multiple existing data sets. 

Provide data sets and documentation for data management decisions, and participate as appropriate in making decisions. 

Write programs to create summary data displays and perform data analysis as specified in the statistical analysis plan. 

Use sas, or alternative software, to generate documents (e.g. tables, listings, figures, define.doc, narratives) that can be submitted to regulatory agencies.  

Evaluate results in light of good clinical practice. 

Conduct quality control checks on programs and outputs generated by statisticians and other programmers. 

Write and check codes, as well as output checks and comparisons in accordance with standard operating procedures. 

Identify training needs and assist in the implementation of training activities for self and other staff.