Senior Statistical SAS Programmer – Kenya (home-based roles)

IQVIA’s Real World Evidence Solutions (RWES) group is recruiting Senior Statistical Programmers to join our dynamic team in EMEA.

Closing date for applications is Friday the 16th of April. Applications must be in English to be considered



The RWE Senior Statistical Programmer jobs will provide experienced statistical SAS programming leadership, expertise and consulting to develop process methodology for the department to meet internal and external client needs. In addition, planning and co-ordination of integrated SAS programming solutions serving the full spectrum of statistical programming for often complex projects is key.

These Senior SAS programmer jobs are exciting new solution-driven career enhancing roles within the team as RWES expands into developing further innovations for clients.

Day to day responsibilities of a Senior Statistical Programmer with RWES:

The Senior SAS Programmer will perform, plan co-ordinate and implement the following for complex studies: (i) the SAS 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
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 Statistical Programming department for complex studies
Fullfil 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 understanding of requirements and timelines
Estimate programming scope of work, manage resources, communicate project status and negotiate/re-negotiate timelines for deliverables
Use and promote established standards, SOPs and best practices
Provide training and mentoring Statistical Programming team members

Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries
Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
Strong knowledge of SDTM structures and ADaM standards
Leadership experience as technical team lead and project lead
Directly engaging with clients
Masters Degree in computer science or related field and 3 years relevant experience; Bachelor’s degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience
In-depth knowledge of applicable regulatory requirements; i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Good organizational, interpersonal, leadership and communication skills
Ability to independently manage multiple tasks and projects
Ability to delegate work
Excellent accuracy problem-solving skills
Recognizes when negotiating skills are needed and seeks assistance
Ability to establish and maintain effective working relationships
Already possess the right to work in the recruiting country without the need for a visa/sponsorship

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


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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, including consulting services. It has a network of more than 58,000 employees in more than 100 countries.As of 2017, IQVIA was reported to be one of the world's largest contract research organizations