SAS Programmer

Highly Competitive Salary
  1. Permanent
  2. Programming
  3. United States
Bedminster, New Jersey
Posting date: 27 Jun 2019
BM.JC.24072_1561647180

ProClinical is currently seeking an SAS Programmer for a for a global specialty pharmaceutical company located in Bedminster, NJ. Successful candidate will be responsible for supporting the Senior and Principle SAS programmer on designing, developing, validating, and maintaining data sets, reporting, general purpose and ad hoc SAS programs used in the support of regulatory submission of clinical trials, or internal decision making relative to clinical trial conduct.

Job Responsibilities

  • Generating and validating tables, listings, and figures per protocol and statistical analysis plan and for ad-hoc requests.
  • Validating SAS programs written by others.
  • Assisting management in maintaining SOPs and work instructions relevant to SAS programming.
  • Following regulatory requirements and guidelines for the development, usage, and maintenance of programs to support regulatory submissions.
  • Completing duties assigned on-time and accurately.
  • Writing and maintaining documentation to describe program development, logic, coding, testing, and updating.
  • Supporting departmental archiving of computer programs, data, and documentation.
  • Creating and executing SAS programs to extract data from databases and create analysis-ready SAS datasets.
  • Converting external data to SAS datasets for internal use.
  • Assisting in designing robust, flexible, and modular macros for projects.

Skills and Requirements

  • BS or BA in Computer Information System, Computer Science, Mathematics, Statistics, or a related field.
  • 5 years of SAS programming experience in life sciences or medically related environment.
  • Working knowledge of CDISC SDTM, ADaM, Define.xml, CFR 21 Part 11 compliance, ICH and FDA standards preferred.
  • Strong knowledge of BASE/SAS, SAS Macros, ODS and SAS/Graph in a Windows SAS environment.
  • Knowledge of data manipulation, report generation in support of regulatory submission.
  • Understanding of data and system dependencies, validation techniques, and integration of studies for ISS/ISE.
  • Knowledge of MS-Office.
  • Technical writing skills adequate to prepare effective documentation for programs and contribute to SOP development.
  • Effective interpersonal skills in collaborating with teams composed of individuals with widely diverse backgrounds, skill levels, and organizational levels.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Junis Citozi at (+1) 929-388-1650 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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