Senior SAS programmer

Highly Competitive Salary
  1. Permanent
  2. Programming
  3. United States
Princeton, New Jersey
Posting date: 13 May 2019
SS.JC.23319_1557761536

ProClinical, in support of our client, are seeking an individual to fill the role of Senior SAS Programmer, based in Princeton, NJ.

Responsibilities

  • Lead statistical programming activities as Trial Programmer for 1-2 studies or assigned project level activities.
  • Coordinate activities of all programmers either internally or externally.
  • Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects.
  • Review eCRF, discuss data structures and review activities as member of the Data Review Team.
  • Comply with company, department and CDISC standards and processes, and review and develop programming specifications as part of the analysis plans.
  • Provide input into statistical programming solutions and/or ensure their efficient implementation.
  • Ensure timely and quality development and validation of datasets and outputs for CSRs, regulatory submissions/interactions, safety reports, publications or exploratory analyses (as required) in the assigned drug development study/project according to specifications.
  • Responsible for end-to-end development of a macro or utility function, or at least one local project under supervision.
  • Maintain up-to-date knowledge of programming software, as well as CDISC requirements.

Skills and Qualifications

  • BA/BS/MS in related scientific field and 3-4 years of work experience in a programming role preferably supporting clinical trials/ or in pharmaceutical industry.
  • Good SAS experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate deliverables.
  • Knowledge of CDISC data structures as well as a solid understanding of the development and use of standard programs.
  • Good understanding of regulatory requirements relevant to Statistical Programming and clinical study practices, procedures and methodologies.
  • Proven ability to produce timely and quality deliverables under guidance.

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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