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Principal Statistical Programmer
Principal Statistical ProgrammerIQVIA • Durham, North Carolina, USA
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Principal Statistical Programmer

Principal Statistical Programmer

IQVIA • Durham, North Carolina, USA
[job_card.30_days_ago]
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  • [job_card.full_time]
  • [job_card.part_time]
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Internal Job Description

Location : Homebased anywhere in the US

Purpose :

Join our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services including specifications and user needs analysis for complex project or client requirements.

Job Details :

  • Position : Principal Statistical Programmer
  • Home Based
  • Min 7 years of CRO / Pharma Industry
  • TherapeuticAreas : Oncology / / Immunology / / IDV / / EDCP

Key Skills :

  • Must have expertise of R programming as well as SAS Base and good knowledge of SAS graph and SAS Macros.
  • Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician.
  • Must have excellent knowledge of CDISC standards (SDTM andADaM)
  • Thorough understanding of relational database components and theory.
  • Excellent application development skills.
  • Strong understanding of clinical trial data and extremely hands on in data manipulations analysis and reporting of analysis results.
  • Good understanding of ICH E6 ICH E3 ICH E8 ICH E9 and clinical research processes.
  • Minimum of 7 years of experience in Statistical Programming in pharmaceutical or medical devices industry
  • Good verbal and written communication skills.
  • Ability to work on multiple projects plan organize and prioritize activities.

    • Required Knowledge Skills and Abilities :

  • Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
  • In-depth knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Knowledge of statistics programming and / or clinical drug development process
  • Advanced knowledge of R programming
  • Base SAS SAS / STAT SAS Graph and SAS Macro Language
  • Should have experience with SDTM Implementation andADaMimplementation according to CDISC Standards.
  • Must have expertise in SAS / BASE SAS / MACRO SAS / STAT SAS / GRAPH SAS / ACCESS SAS / ODS SAS / SQL.
  • Good organizational interpersonal leadership and communication skills
  • Ability to independentlymanage multiple tasks and projects
  • Ability to delegate work to other members of the SP team
  • Excellent accuracy and attention to detail
  • Ability to delegate work to other members of the SP team SPM
  • Exhibits routine and occasionally complex problem-solving skills
  • Ability to lead teams and projects and capable of managing at a group level
  • Recognizes when negotiating skills are needed and seeks assistance.
  • Ability to establish and maintain effective working relationships with co-workers managers and clients.

    • Responsibilities :

  • Perform plan co-ordinate and implement the following for complex studies : (i) the programming testing and documentation of statistical programs for use in creating statistical tables figures and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..
  • Ability to interpret project level requirements and develop programming specifications as appropriate for complex studies.
  • Provide advanced technical expertise in conjunction with internal and external clients and independently bring project solutions to SP teams and Statistical Programming department for complex studies.
  • Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
  • Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.
  • Estimate programming scope of work manage resource assignments communicate project status and negotiate / re-negotiate project timelines for deliverables.
  • Use and promote the use of established standards SOP and best practices.
  • Provide training and mentoring to SP team members and Statistical Programming department staff.

    • MINIMUM REQUIRED EDUCATION AND EXPERIENCE :

  • Bachelors degree from reputable university preferably in science / mathematics related fields

    • IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at

    IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $88300.00 - $294800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and / or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and / or other forms of compensation may be offered in addition to a range of health and welfare and / or other benefits.

    Required Experience :

    Staff IC

    Key Skills

    Business Development,Customer Service,Attorney,CISSP,Data Analysis

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

    Monthly Salary Salary : 88300 - 294800

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