Description:
Seeking a Senior Statistical Analyst to be a member of the clinical
project for this successful biotech company. You will be responsible
for the design, development, implementation, and maintenance of
software for the monitoring, reporting, and analysis of clinical
trials. Develop software to monitor ongoing studies, produce data
listings, summary tables, graphics analyses and publication. Integrate
data across studies; provide consistency within a project, database
design, analysis files, tables, listings, and graphs. Test, document,
review and validate all programs according to departmental guidelines.
Review the CRF design, data management, and statistical analysis plans
for impact on software systems and study analyses. Do enhancements and
/ or new features for applications. Develop specifications and coding
for new standardized clinical software tools.
Requirements:
Minimum 4 years of SAS programming with a BS in statistics, math, or 2
years with an MS in a related field. Skilled in SAS programming
language, data step programming and report writing and macro writing.
Skilled in use of graphics software (SAS/Graph, S-Plus. Knowledge of
advanced statistical procedures in SAS (Lifeset, Mixed, Glm).
Knowledgeable in data base theory, relational database concepts and
Oracle Clinical. Ability to interact effectively with members of other
functional teams. A working knowledge of basic statistics for
communicating effectively with biostatisticians. Some experience with
data warehouse design and implementation and database design.
Understanding of regulatory guidelines, SAS to process, report, and
analyze clinical trial data, understanding of the drug approval
process. Knowledge of regulatory filing desirable but not required.
Email resume for immediate consideration, or for further information
please contact:
Tom Whiting
Enterprise Resource Group
San Francisco, CA
(voice) (415) 221-6300
(email) [EMAIL PROTECTED]
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