Job content will be varied and includes statistical analysis of clinical trials, efficacy analysis, PK-PD analysis, ...
As a statistical programmer you will be in charge of the statistical analysis of studies.
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.
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.
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.
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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You can also send a spontaneous application including your resume to email@example.com