Background information about the job or company (e.g., role context, company overview)

IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...

Responsibilities or duties

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 to 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

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

Qualifications or requirements (e.g., education, skills)

Bachelor's Degree in Maths, Computer science, Statistics, or related field

Strong Efficacy experience

Advanced knowledge of statistics, programming and/or clinical drug development process

Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language

Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)

Experience needed

7+ years’ Statistical Programming experience within the Life Science Industry

Any other provided details (e.g., benefits, work environment, team info, or additional notes)

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• 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 to 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
• 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

• Base SAS
• SAS Graph
• SAS Macro Language
• CDISC/ADaM/SDTM

• Bachelor's Degree in Maths, Computer science, Statistics, or related field
• Strong Efficacy experience
• Advanced knowledge of statistics, programming and/or clinical drug development process
• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language
• Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)