RPS
Career Opportunity
Title: Biostatistician
Reference
Number: 33554
Location: New
Jersey
| The biostatistician will serve as a statistician for one or more study protocols. Responsibilities will include some or all of the following: contribute to study design as a member of the protocol team, develop statistical analysis plans, perform complex statistical analyses, and collaborate on final analysis and submission/manuscript preparation. |
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Write and review the statistical analysis plan (SAP) for phase II – IV. |
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Assure the statistical validity and completeness of the case report form design process. |
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Review (validate) the statistical analysis and the analysis programs. |
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Provide statistical guidance in development of clinical research program and in design of individual studies as part of multi-disciplinary team; responsible for statistical input to protocol. |
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Perform and/or review sample size calculations. |
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Develops plans and provides SAS programming support for analysis Tables, Listings, and visual displays of data collected in clinical studies. |
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Must have
at least 3 years experience as a Biostatistician working in a
clinical environment.
Background in statistical computing within a clinical trial
setting required including proficiency with SAS. MS or
Ph.D. The
ability to work under tight deadlines while maintaining high
standards.
Must be cooperative, team-oriented and
proactive |