Statistical Programmer

Description

Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways to support lead programmer in generation of analysis datasets, generation of TLGs (Tables, Listings, and Graphs), validation of aforementioned data and reports, and maintenance of study documentations.

Work Experience:

• 2-5 years related experience.
• Experience is within the pharmaceutical/biotech industry or relevant clinical research organization Industry.
• Experience in programming with a regulated environment.

Functional/Technical Knowledge & Skills (including any required proficiency for particular computer programs or applications, if applicable):

A knowledge of SAS System Software not limited to but must meet at a minimum

Data manipulations using a SAS data step.

Basic knowledge of SAS BASE Procedures such as PROC SORT and PROC FREQ

Basic knowledge of SAS STATS Procedures such as PROC LIFETEST

Basic knowledge of SAS MACRO Facility to call department macros and use defined macro variables.

How to perform a SAS merge.

Detailed knowledge of SAS date and time function and manipulations.

Specifications writing experience a plus

Customer & Industry Knowledge:

• Previous knowledge should be in the pharmaceutical/biotech industry clinical research organization Industry.
• Oncology experience a plus, especially efficacy
• Basic knowledge with the drug development process
• Basic knowledge of ICH, FDA, and GCP regulations and guidelines
• Basic knowledge of CDISC/SDTM and ADaM standards a plus

Education/Training:

• BS/BA/MS in Statistics, Computer Sciences, Mathematics, or Life Sciences, or equivalent experience

To find out more about Real please visit www.realstaffing.com