Assoc Stat Programmer
IQVIA
Bengaluru, KA, India
2d ago
source : CareerArc Group LLC

Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.

Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

PURPOSE

Provide programming expertise to develop and maintain programs to meet internal and external clients' needs. Provide and assist in the development of project-related solutions to a wide range of statistical programming tasks.

RESPONSIBILITIES

  • Perform (i) the programming, testing, and documentation of programs for use in creating statistical tables, listing and figures summaries, (ii) the programming, testing and documentation of analysis dataset (derived datasets) and transfer file for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically.
  • Detect errors in detail and corrects them (e.g., reviews tables / listings, edit checks output and SAS programs to ensure quality of deliverable)
  • Assist in the development of programming documentation including specifications, as appropriate, under supervision.
  • Provide advanced technical expertise in conjunction with internal and external clients, and bring project solutions to teams and department, under supervision.
  • Develop, implement and validate new process technologies, macros and applications under supervision.
  • Fulfill project responsibilities at the level of assisting the statistical programming team lead.
  • Understand timelines for and milestones affecting their work and alert supervisor to potential slippage
  • All responsibilities are essential job functions unless noted as nonessential (N).

    REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Knowledge of programming, statistics and / or clinical drug development process
  • Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Working knowledge of computing applications such as Base SAS, SAS / STAT and SAS Macro Language
  • Organizational, interpersonal and communication skills
  • Ability to effectively handle multiple tasks within a project, under supervision
  • Excellent accuracy and attention to detail
  • Aptitude for mathematical calculations
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Masters degree in computer science or related field; Bachelor's degree t in biostatistics or related field and 1 year relevant experience;
  • or equivalent combination of education, training and experience

    Join Us

    Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare.

    Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

    Forge a career with greater purpose, make an impact, and never stop learning.

    Apply
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