Senior Statistical Programmer at IQVIA

Job Description
Join us on our exciting journey!

Job Overview:

• As a Senior Statistical Programmer, you will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients’ needs.
• Plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
• You will also provide technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Key Responsibilities:

• Perform, plan co-ordinate and implement the following for complex studies:
• The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing
• The programming of analysis datasets (derived datasets) and transfer files for internal and external clients
• The programming quality control checks for the source data and report the data issues periodically
• 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.
• Provide training and mentoring to SP team members

Requirements:

•  5+ years Statistical Programming experience within the Life Science industry
•  BSc or MSc degree in Biostatistics or related field
• Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
•  Ability to implement more advanced statistical procedures as per specifications provided by Biostatistician.
• Excellent knowledge of CDISC standards (SDTM and ADaM)
• 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.
• Ability to work on multiple projects, plan, organize and prioritize activities
• 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

Join IQVIA to see where your skills can take you

•  Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being