Flexible location: Reading UK or Strasbourg, France
Hybrid role
Job Overview:
Join our dynamic team as a Clinical Data Programmer and utilize your technical expertise in the exciting field of clinical studies. In this pivotal role, you will have the opportunity to plan and coordinate the implementation of clinical studies, with a special emphasis on data integration.
Responsibilities:
Programming data exports from various sources.
Managing activities on clinical studies.
Creating listings in multiple output formats.
Working primarily with SAS and also using databases.
Qualifications:
Master's degree or equivalent in science/computer science or related field.
2 years of work experience in programming/data management within a biometric department.
Knowledge of InForm and Rave EDC.
Proficiency in safety integration with E2B format.
Understanding of data integration and data lakes.
Excellent organizational, communication, and technical database skills.
Ability to establish and maintain effective work relationships.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com