Quanticate UK - Head Office

  • Senior Programmer I

    Job Locations IN-KA-Bangalore
    Posted Date 3 weeks ago(6/22/2018 11:22 AM)
    ID
    2017-1658
    # of Openings
    1
    Category
    Programming
  • Overview

    We have an exciting opportunity for an experienced Senior SAS Programmer I to join us in India!

     

    This is a multi-discipline role within Quanticate Programming department (our biggest team). This role focuses on providing project and technical support in the preparation and review of high quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients.

    Responsibilities

    • Deliver excellent customer care in support of genuine value and a great customer experience.
    • Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines.
    • Excellent knowledge of pharmaceutical industry standards.
    • Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client.
    • Maintain up-to-date knowledge of the external regulatory environment relating to programming, including ICH/GCP requirements, and provide advice and educate colleagues (and clients) on changes to regulatory requirements and/or other guidelines relating to programming.
    • Provide high quality deliverables and appropriate communication within expected timelines and budget.
    • Provide mentoring, as required.
    • Ability to lead teams, as required.
    • Ability to work with different functions, and across sites as required
    • Ability to review and provide comments on clinical documents, e.g. protocol, CRF and SAP.
    • Ability to perform Peer Review and Final Inspection.
    • Ability to represent the company at external conferences and forums, from a clinical programming perspective.
    • Participate in meetings such as recruitment, business development and audits from a clinical programming perspective.
    • Perform other reasonable tasks as requested by management.
    • Follow appropriate Project Management procedures.
    • Advanced programming experience covering activities from study set-up to final reporting.

    Qualifications

    • Qualified to minimum MSc level
    • Relevant experience within the pharmaceutical or medical sector
    • Good PC skills including working knowledge of Microsoft Office
    • Experience using SAS and other statistical software
    • Good written and oral communication skills
    • Good organisational skills
    • Good analytical and problem solving skills
    • Strong interpersonal skills

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