What are your responsibilities?

To participate to Phase I-IV Clinical Development activities within a program or group of related programs within the context of the internal process in order to ensure the high quality and on-time delivery of all clinical data that will allow world-wide registration in compliance with the clinical development plan, good clinical practices (GCP), and internal standard operating procedures (SOP).
Key Responsibilities:

1. Participate in Clinical Development activities for a study or a number of studies within a specific program or group of related programs.
2. Serves as a scientific and management reference for the project (internally/externally)
3. As a member of the Clinical Project Team, always actively participate and engage within the project matrix.

4. Actively participate in preparing the clinical portion of the regulatory files and the registration process

5. Provides support to Marketing/Business Development throughout product life cycle

6. Show active follow-up the product-related Environment

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