This is a brilliant opportunity for an established Senior Statistical Programmer to join an exceptional and dynamic programming group. We seek someone willing to move from one Senior Statistical Programming role to another in return for the experience and unrivalled career progression Iqvia can offer. We ask you only apply if you match or exceed the candidate criteria below.
UK visa sponsorship is NOT available for this role.
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. 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! Come join us on this exciting journey!
Job Overview:
You will know as a Senior Statistical Programmer you'll provide experienced technical expertise and leadership 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. You will provide technical expertise and leadership to the department and provide internal consulting services such as 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.
Essential Requirements:
- Already be an established Senior Statistical Programmer
- 5+ years Statistical Programming experience within the Life-Science industry
- Experience in SAS Base, and good knowledge of SAS graph and SAS Macros
- Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
- Ability to implement more advanced statistical procedures as per specifications provided by Biostatisticians.
- Excellent knowledge of CDISC standards (SDTM and ADaM)
- Thorough understanding of relational database components and theory
- Excellent application development skills
- 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
Embrace your curiosity and grow your career in an exciting environment where development is a priority.
Think boldly and disrupt conventional thinking.
Enjoy what you do.
Whatever your career goals, we are here to ensure you get there!
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. Learn more at https://jobs.iqvia.com
