Qualified Applicants will possess: |
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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. |
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| One Main Street Chatham, NJ 07928 USA Phone: 1.973.635.9898 Fax: 1.973.635.9881 |