Senior SAS Programmer

Highly Competitive Salary
  1. Permanent
  2. Programming
  3. United States
Bedminster, New Jersey
Posting date: 03 Jun 2019
SS.JC.23704_1559581059

ProClinical is currently seeking a Senior SAS Programmer for a global specialty pharmaceutical company. The successful candidate will be responsible for 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

  • Generate and validate tables, listings, and figures per protocol and statistical analysis plan and for ad-hoc requests.
  • Validate SAS programs written by others.
  • Assist management in maintaining SOPs and work instructions relevant to SAS programming.
  • Follow regulatory requirements and guidelines for the development, usage, and maintenance of programs.
  • Write and maintain documentation to describe program development, logic, coding, testing, and updating.
  • Support departmental archiving of computer programs, data, and documentation.
  • Create and execute SAS programs to extract data from databases and create analysis-ready SAS datasets.
  • Convert external data to SAS datasets for internal use.
  • Design robust, flexible, and modular macros for projects.
  • Assist in timeline set up and ensures that programming activities are implemented consistently across clinical studies

Skills and Requirements

  • BS or BA in Computer Information System, Computer Science, Mathematics, Statistics, or a related field.
  • 7+ years of SAS programming experience in life sciences or medically related environment.
  • 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.

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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