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Job Information
Job title

SAS STATISTICAL PROGRAMMER

Company Nation Hire
Wage between $0.00 - $0.00 Annually
Location United States, California, Irvine
Employment type Full Time
Education Bachelor
Year Experience 3 - 4 Years of Practical Experience
Travel None
Published on 8/23/2007
Description
SAS STATISTICAL PROGRAMMER

WE ARE SEARCHING FOR A FULL TIME SAS STATISTICAL PROGRAMMER IN THE BIOMEDICAL RESEARCH FIELD =E2=80=A6 IS THAT YOU?

Our client is a leading edge biopharmaceutical company that acquires, develops and commercializes a diversified portfolio of oncology and other drug candidates that meet critical health challenges for which there are few other treatment options. Their expertise lies in identifying undervalued drugs with demonstrated safety and efficacy, and adding value through further clinical development and selection of the most viable and low-risk methods of commercialization.

The companys pipeline includes promising early and late-stage drug candidates with unique formulations and mechanisms of action that address the needs of seriously ill patients, such as at-home chemotherapy and new treatment regimens for refractory disease. The passion of the company to identify, develop and deliver better options for people suffering from cancer is behind every action they take.

What is in it for you?
They generously compensate their staff members and provide a magnificent health, dental, vision, life, AD&D, and long-term disability insurance package, as well as a 401k plan with matching Company stock.

What are they looking for?
Develop SAS programs for data cleaning and reporting. Create customized listings/reports with SAS. Provide statistical programming support under the direction of the senior staff for the creation and maintenance of analysis data sets, tables, listings, and figures.

Responsibilities:
- Create derived analysis datasets.
- Execute analyses specified in the Statistical Analysis Plan (SAP) under the
guidance of the project statistician.
- Act as primary programmer to produce tables, listings, and figures (TLFs) for the clinical study report (CSR) and ad-hoc reports.
- Act as secondary programmer to validate SAS programs that produce derived analysis datasets and data analyses and ad-hoc reports.
- Assist Clinical Data Management (CDM) group to design or review database structures, and provide CRF listings for edit check purposes.
- Develop and Refine SOPs for data handling, programming and system validation.


Qualifications, Education and Experience:
- Degree in Life Sciences, Computer Science, Statistics, or related field.
- General knowledge of medical terminology and clinical trial methodologies.
- Bachelor degree with a minimum 6yrs SAS programming experience or a Masters or equivalent degree with 4 yrs SAS programming experience.
- Strong SAS programming skills with proficiency in SAS/Base, SAS Stat, and SAS Macros with basic understanding of SAS/Graph.
- Prior experience working in the pharmaceutical/Biotechnology industry.
- Ability to work independently
- Clear verbal and written communication skills; able to work with other cross function areas and CROs.
- Excellent collaborative skills and the ability to manage complexity and change in a dynamic environmentdf-tc

Experience/Skills
See above

Other desired skills:
Statistical Programmer
This job has expired.