Principal - Statistical / (SAS) Development
Company Name:
Talon
Our client, located in Fort Lee, NJ is seeking a Senior Statistical (SAS) Programmer for an immediate full-time position. Details include:
This is a position for a hands on Sr. Statistical (SAS) Developer. It has Manager level role.
-Summary of Responsibilities Provide statistical programming support to clinical trials for regulatory submissions and various publications posters etc.
-Support the Biostats function in statistical analysis including generating analysis data sets, patient listings, tables and figures for clinical trials.
-Develop and maintain the infrastructure for project files of SAS datasets and SAS codes
Essential Functions
-Develop SAS programs to produce analysis datasets.
-Write/Review data definition tables, data specs or related documents.
-Design /develop SAS macros and other utulities to expedite SAS programming activities.
-Knowledge and Skills: Indicate the education level, previous experience, specific knowledge, skills and abilities required to meet minimum requirements for this position.
Minimum education requirements
-Masters
Experience required
-5 - 7 Years
Knowledge & skills (general and technical)
-Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO
-Extensive experience in creating data tables, figures and listings. documents and the analysis necessary to support electronic submissions and publications.
-Working familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines.
(FDA/CFR, ICH/GCP
Estimated Salary: $20 to $28 per hour based on qualifications.
Talon
Our client, located in Fort Lee, NJ is seeking a Senior Statistical (SAS) Programmer for an immediate full-time position. Details include:
This is a position for a hands on Sr. Statistical (SAS) Developer. It has Manager level role.
-Summary of Responsibilities Provide statistical programming support to clinical trials for regulatory submissions and various publications posters etc.
-Support the Biostats function in statistical analysis including generating analysis data sets, patient listings, tables and figures for clinical trials.
-Develop and maintain the infrastructure for project files of SAS datasets and SAS codes
Essential Functions
-Develop SAS programs to produce analysis datasets.
-Write/Review data definition tables, data specs or related documents.
-Design /develop SAS macros and other utulities to expedite SAS programming activities.
-Knowledge and Skills: Indicate the education level, previous experience, specific knowledge, skills and abilities required to meet minimum requirements for this position.
Minimum education requirements
-Masters
Experience required
-5 - 7 Years
Knowledge & skills (general and technical)
-Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO
-Extensive experience in creating data tables, figures and listings. documents and the analysis necessary to support electronic submissions and publications.
-Working familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines.
(FDA/CFR, ICH/GCP
Estimated Salary: $20 to $28 per hour based on qualifications.
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