Pharmaceutical Statistical Analyst- Clinical Trials - (US-PA-Swiftwater - 18370)

Minimum Education: Tech School
Job Type: Full Time
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In this top pharmaceutical company's oncology business unit you will be responsible as a lead statistician. Pharmaceutical Statistical Analyst- Clinical Trials SAS
As a lead statistician you will participate/support development of clinical program. Review the protocols and case report forms for soundness of trial design. Write statistical methodology section of the protocol. Prepare statistical analysis plan and programming specifications. Pharmaceutical Statistical Analyst- Clinical Trials SAS SAS SAS SAS
Perform inferential statistical analyses. Write the statistical section of the clinical trial report and review clinical trial report. Support/participate in drug project related activities including preparation of global HA submissions. Oversee CRO statistical and programming deliverables for trials contracted out.
Solid hands-on experience as a lead statistician in clinical development programs a plus. Experience in protocol development, analyses and clinical trial reports/publications of Phase II-IV clinical trials. Good knowledge of drug development process. Very good oral and written communication skills. Knowledge of FDA/ICH guidelines. Good knowledge of SAS computer package. Pharmaceutical Statistical Analyst- Clinical Trials SAS
SAS Programming. SAS Certification Preferred. SAS Clinical Trials exp a must.



Requirements: Masters 1 to 2 years pharmaceutical experience