Senior/Clinical Data Review Programmer (SAS or Spotfire): Real World Evidence – home based or hybrid
The vision of our Real-World Evidence 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 Real-World Global Biostatistics & Programming team delivers insightful analytics for predominantly primary data collection studies, and we 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!
Perform SAS and/or Spotfire Programmer responsibilities on multiple projects while maintaining a guiding role within the department. Develop and validate programs to generate data cleaning reports and prepare data extracts. Develop internal tools and add-ons to facilitate the processes and work flow for Project Programming, and other departments within Data Operations. Provide programming support to project team members and others within Project Programming.
**PLEASE APPLY WITH YOUR CV IN ENGLISH**
**CANDIDATE CRITERIA – EDUCATION, KNOWLEDGE, SKILLS AND EXPERIENCE**
+ BS degree/Masters (or equivalent, based upon education and experience) in Computer Science, Mathematics, life/analytical sciences or related field
+ **4 years of work experience in SAS and/or Spotfire programming, preferably in a clinical data management or biostatical environment**
+ Excellent knowledge of SAS Base, SAS Macro, ODS and Spotfire as well as strong data step skills
+ Knowledge of programming and validation methods, and software development life cycle
+ Knowledge of relational database concepts, and SQL experience
+ Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research
+ Ability to perform multiple highly detail-oriented tasks with no supervision while meeting deadlines
+ Ability to learn new programming languages, technology and tools
+ Able to train and mentor junior staff
+ **Already possess the right to work in the hiring countries indicated**
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
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