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.
Would you like to join us?
You can also send a spontaneous application including your resume to firstname.lastname@example.org