Senior Statistical Programmer

4 days ago

Copenhagen, Copenhagen, Denmark IQVIA Full time

Job Overview:

As a Senior Statistical Programmer at IQVIA, you will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients' needs. Your key responsibilities will include planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs.

Responsibilities:

• Perform, plan, coordinate, and implement the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing.
• Program analysis datasets (derived datasets) and transfer files for internal and external clients.
• Program quality control checks for the source data and report data issues periodically.

• Interpret project-level requirements and develop programming specifications 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 of 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.

Benefits:

• 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.

Join IQVIA:

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. At IQVIA, you will have the opportunity to work with a diverse, global team and harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

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