ERT

  • SAS Programmer (Systems Analyst 1)

    Job Location US-PA-Philadelphia | US
    Shift
    40
    Type
    Regular Full-Time
  • Overview

    Join us in our Philadelphia office as a SAS Programmer (Systems Analyst) where you will create and test SAS code used for non-standard data file creation, mentor System Analyst I staff and be aprogramming resource for CSO staff and other departments as needed.

     

    ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that our customers can move ahead with confidence. With more than 45 years of clinical and therapeutic experience, ERT balances knowledge of what works with a vision for what’s next, so it can adapt without compromising standards.

    Powered by the company’s EXPERT® technology platform, ERT’s solutions enhance trial oversight, enable site optimization, increase patient engagement, and measure the efficacy of new clinical treatments while ensuring patient safety. Over the past four years, more than half of all FDA drug approvals came from ERT-supported studies. Pharma companies, Biotechs, and CROs have relied on ERT solutions in 9,500+ studies spanning three million patients to date. By identifying trial risks before they become problems, ERT enables customers to bring clinical treatments to patients quickly – and with confidence. For more information, go to ert.com or follow us on LinkedIn, Twitter, and Facebook.

    Responsibilities

    ESSENTIAL DUTIES AND RESPONSIBILITIES:

    1. Perform any and all functions of the System Analyst I as required to meet corporate commitments and deliverables; in particular, to review or provide standard data specifications and create standard data files through SAS. 
    2. Receive and review non-ERT standard client file specifications from Data Manager / Project Manager or client and interact with the client to finalize transfer specifications 
    3. Develop SAS programs to create non-standard data files, specifically vertical file and incremental data file requirements 
    4. As part of the Software Development Life Cycle, review User Requirements and create and/or review Functional and Technical Specifications and approve specifications 
    5. Create and test ad-hoc programs for:
      • Esoteric quality control checks requested by QC
      • Data resolution/mining
      • Other client requirements

    OTHER DUTIES AND RESPONSIBILITIES: 

    1. Assist with orientation and training of Systems Analysts and Data Management / Project Management personnel as determined by management. 
    2. In conjunction with the entire department, recommend, develop and implement SOPs for improved CDP Procedures.  

    The duties and responsibilities listed in this job description represent the major responsibilities of the position.  Other duties and responsibilities may be assigned, as required.  ERT reserves the right to amend or change this job description to meet the needs of ERT.  This job description and any attachments do not constitute or represent a contract.

    Qualifications

    1. BS in computer sciences or related field; MS in computer sciences related field helpful.
    2. Minimum three years experience in BASE SAS products and procedures and one year experience in database design and data structures.
    3. Understanding of the pharmaceutical drug development process, as gained through a minimum of two years experience in the pharmaceutical or healthcare industry.
    4. Strong organization, analytical and communication skills.
    5. Detail-oriented.
    6. Experience with Windows and Microsoft Office products.
    7. Experience with DB programming is a plus.
    8. Ability to work in a rapidly changing and fast-paced environment, with short timelines.
    9. Adaptable and flexible. Able to work in a frequently high-stress environment.

    We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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