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    Sr Statistical Programmer - Bengaluru, India - Clario

    Clario
    Clario Bengaluru, India

    1 week ago

    Default job background
    Full time
    Description

    Are you seeking a purposeful and rewarding SAS programming career opportunity?

    Our statistical programming team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario

    What we offer:

  • Competitive compensation
  • Attractive benefits (security, flexibility, support and well-being)
  • Engaging employee programs

    • What you'll be doing:

    In the Senior Statistical Programmer role at Clario you will create, test and maintain SAS codes used to create CDISC compliant datasets for the cardiac safety statistical analysis; create and maintain procedures for creation of ADaM datasets and help us create electronic submission packages for cardiac safety submissions.

  • Support statistical programming activities for assigned Cardiac safety studies - Creation of dataset specifications as per study requirements.
  • Participate in process improvement for SAS programming and mentoring of new employees.
  • Perform any and all functions as required to meet corporate commitments and deliverables; in particular, to creating codes for statistical datasets through SAS as well as reviewing and creating the electronic submission deliverables for sponsor submission.
  • Create and maintain SAS codes for analysis datasets, which includes programming analysis specific flags and other specifications per the Statistical analysis plan.
  • Create submission ready datasets for cardiac safety trials (SDTM EG and ADaM ADEG) in coordination with the client, internal statistics and data management teams while being compliant with CDISC standards.
  • Maintain working knowledge of CDISC standards and recommend changes to processes and standard specifications as needed.
  • Create and dataset reviewers guide for FDA submissions with reference to the datasets created for statistical analysis. Assist statisticians in preparation of Tables Listings and Figures for cardiac safety studies.
  • Assist with orientation and training of members of the statistics team, Systems Analysts and Data Management personnel as determined by management.
  • In conjunction with the entire department, recommend, develop and implement SOPs for improved procedures within the Statistics group.

    • What we're looking for:

  • BS in computer sciences, Engineering, Statistics or Mathematics.
  • Experience with CDISC SDTM and ADaM standards.
  • Minimum of 5 years' experience in SAS products and procedures in pharmaceutical or life sciences setting preferred - Understanding of the pharmaceutical drug development process, as gained through a minimum of two years' experience in the pharmaceutical or healthcare industry.
  • Strong organization, analytical and communication skills.
  • Detail-oriented.
  • Experience with Windows and Microsoft Office products.
  • Experience with TFLs generation is a plus.
  • Ability to work effectively in teams, effectively operates within a matrix organization and with multi-disciplinary groups.
  • Excellent team player with strong interpersonal skills contributing to building the team spirit.
  • Ability to understand and anticipate the needs of customers, and respond to their inquiries.
  • Ability to organize team work and prioritize and balance concurrent tasks and responsibilities.
  • Excellent time management skills.
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