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IQVIA MedTech Clinical Solutions, specializes in clinical research for Medical Devices

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IQVIA MedTech’s focused expertise meets the growing needs of device Sponsors to justify product safety and effectiveness as well as reimbursement and adoption challenges due to increased scrutiny by regulators, end-users, and patients.

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.

Function
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 facing international costumers as a first point of contact for data management, 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.

Profile
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. With a Bachelors degree and 1-2 years experience you can also be considered. 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.

Language requirements
​​​​​​​Fluent in English both verbally and in writing