IQVIA Senior Statistical Programmer: Real World Evidence Jobs in South Africa
IQVIA Senior Statistical Programmer: Real World Evidence Jobs in South Africa
Job Description The vision of our Real-World Evidence (RWE) teams is to pioneer and lead with scientific and technical expertise in the generation and dissemination of high-quality Real-World Evidence. We make a true difference to patient lives, globally. Come join us on this exciting journey!
Our RWE Global Biostatistics & Statistical Programming team delivers insightful analytics for predominantly primary data collection studies, and are increasingly supporting innovative studies such as External Comparators, Enriched Studies, and Pragmatic Trials.
We are a highly motivated global team of more than 150 employees, responsible for engaging with our clients early to help shape the statistical analysis of these study designs, contribute to protocols and deliver results to meet their needs.
We have unique opportunities to define the way our clients develop and apply Real-World Evidence for healthcare decision making. So we are looking for the best talent to join us.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of Real-World Evidence in an evolving industry!
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.
You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
Acting as a lead on studies, you will directly communicate with internal
and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as estimating programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.
Please apply in English
Essential Requirements:
5+ years Statistical Programming experience within the Life-Science industry
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 Biostatisticians.
Excellent knowledge of CDISC standards (SDTM and ADaM).
Already possess the right to work in EMEA.
Thorough understanding of relational database components and theory.
Excellent application development skills.
Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team.
Bachelors or Masters’ in Computer Science, Mathematics or equivalent.
In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice.
(GCP) and International Conference on Harmonization (ICH) guidelines.
How to Apply
For more information and job application details, see; IQVIA Senior Statistical Programmer: Real World Evidence Jobs in South Africa
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