Jobs

(BIO-)STATISTICIAN

Job content will be varied and includes statistical analysis of clinical trials, efficacy analysis, PK-PD analysis, ...

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STATISTICAL PROGRAMMER

As a statistical programmer you will be in charge of the statistical analysis of studies.

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DIAGNOSTIC RADIOLOGIST

Medical Imaging is an integral component of oncology clinical trials design. As a Radiologist you will be in charge of reviewing and interpreting diagnostic imaging procedures, namely CT and MRI scans performed at different time points in clinical trials incorporating Imaging endpoints.

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CLINICAL TRIAL ASSISTANT

As a Clinical Trial Assistant, your main responsibilities are to assist in all project/study-specific activities of Biometrics, Medical monitoring and Central Imaging Reading.

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PROJECT MANAGER

As a Project Manager, your main responsibilities are to manage and coordinate all project/study-specific activities of the Biometrics, Medical monitoring and Central Imaging Reading departments.

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MEDICAL WRITER

As a Medical Writer, you will have the end-to-end responsibility for medical writing aspects of clinical studies. This includes contribution to Clinical Study Protocols, Clinical Study Reports, amendments, and manuscripts.

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Would you like to join us?

You can also send a spontaneous application including your resume to recruitment@dice-cro.com