Real World Evidence Statistical SAS Programmer II careers. Exciting new solution-driven jobs based at home (or possibly office based)

IQVIA’s Real World Evidence Solutions group is recruiting Statistical Programmers with great SAS programming skills to join our dynamic Statistical Programming team.

Closing date for SAS Programmer II applications is Sunday the 21st of March. Applications must be in English to be considered.

PURPOSE:

As an RWE Statistical SAS Programmer II you’ll provide statistical programming and data harmonization (for primary and secondary data from - EMRs, PROs, eCRF, Observational studies, etc.) expertise. You’ll advise on database design, data collection and programme tables, listings and figures using SAS (Base SAS, SAS/STAT and SAS Macro) and other applications.

These are exciting new roles as RWE expands into developing further innovations for clients.

RESPONSIBILITIES:

• Develops, executes and reviews programs to provide statistical programming support for statisticians and clients to source, organize (creating statistical TLFs and graphs) and interpret complex data sets
• Conducts statistical analyses for client reports and publications. Utilize findings and insights for practical application to further business operations.
• Innovate for solution and product development
• Report directly to external and internal clients
• Perform programming quality control checks for source data and report issues
• Review tables/listings, edit checks output and SAS programs to ensure quality of deliverables
• Assist in the development of programming documentation including specifications
• Provide advanced technical expertise in conjunction with internal and external clients, and bring project solutions under supervision
• Develop, implement and validate new process technologies, macros and applications under supervision
• Assist the statistical programming team lead to fulfil project remit
• Understand timelines and milestones and alert manager to potential slippage
• Act as technical lead and plan from time to time

MINIMUM SKILLS, EXPERIENCE & QUALIFICATIONS:

• Good knowledge of statistics, programming and/or clinical drug development process
• Good knowledge of Base SAS, SAS/STAT and SAS Macro Language
• Bachelor's/Masters Degree in Computer Science or related field and 3 years relevant experience or equivalent combination of education, training and experience  
• Already possess the right to work in the recruiting country
• 3 years working knowledge of the ADaM standards in clinical trials
• 3 years experience of TLFs in clinical trials
• Working knowledge of the SDTM structure
• Experience programming across a broad range of clients without over reliance on client supplied macros
• Knowledge of applicable clinical research regulatory requirements would be an advantage; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Ability to implement programming specifications as appropriate
• Ability to estimate programming scope of work and assist in communicating project status
• Ability to recognise when negotiating skills are needed and seek assistance when required
• Excellent accuracy and attention to detail
• Ability to handle multiple tasks and projects
• Ability to establish and maintain effective working relationships with co-workers, managers and clients

WE OFFER:

• Competitive salary and benefits package
• Excellent career development
• The opportunity to be part of a friendly and supportive team
• Opportunity to work on complex trials in challenging therapeutic areas

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At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.