Full-time Programmer

2 weeks ago

Vancouver, Canada 30.01 Premier Research Group (India) Private Limited Full time
h3>Senior Principal Programmer - India

Apply locations India time type Full time posted on Posted 2 Days Ago job requisition id R4201 Premier Research is looking for a Senior Principal Programmer - India to join our Biostatistics team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are Built for You. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
    • Develops SAS programs to generate listings with/without shells and to generate CDISC and other analysis data sets as outlined by respective specifications and prepares specifications for CDISC and other analysis data sets.
    • Performs quality control (source code review, double-programming and log review) of SAS programs and assists Data Management with SAS programming needs.
    • Develops and maintains overall awareness in the field of Biostatistical programming by attending training classes, professional meetings, following-up on technical developments, etc.
    • Keeps detailed records of time spent on each project for accurate tracking of project revenue and backlog and ensures that work is completed on time, project hours are tracked at the correct level of quality.
    • Participates in efforts for efficiency and productivity in the department and participates in corporate initiatives and actions that ensure the continued success of the company.
    • Handles complicated or non-standard sources of data and acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team.
    What we are searching for:
    • Educational Background - BS or equivalent from accredited college or university, in statistics, IT, mathematics or closely related field or work related experience to be able to perform this role.
    • Knowledge of ICH and local regulatory authority drug research and development regulations preferred.
    • Advanced knowledge of SAS Software data set architecture, utilities, and programming techniques, advanced SAS macro development and code generation/management algorithms.
    • Demonstrated working knowledge of basic clinical trial design and analysis principles.
    • Working knowledge of CDISC standards and application of these standards to projects.

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