You are responsible for the review of the clinical data, the preparation of the data clarification forms (DCF) / online queries, the tracking and follow-up of the DCFs / queries until resolution and database update. In addition, you perform database testing activities, keep the relevant parties informed about the project objectives and timelines, assists the Clinical Data Manager where possible and you report to all involved parties on a regular basis.
You are responsible for the validation and review of the clinical research data, the creation and follow-up of online queries; to ensure complete, accurate and consistent data for (statistical) analysis. Additional responsibilities include running a variety of scheduled and ad hoc listings, summaries and other data reports upon request by our clients. In addition, you will be involved in database testing activities, assist the Clinical Data Manager with the creation of all Data Management related documents and you report to all involved parties on a regular basis.
By preference, you have a Master in Science (biomedical, biology, pharmacy, etc.), and a first experience in clinical data management is an added value though not a requirement.
You have excellent planning and organizational skills and an eye for detail. Relevant knowledge MS Office is required, knowledge of SPSS would be an asset.
Fluent in English (and Dutch) both verbally and in writing
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.