Michał Szkatuła

Since June 2017 Senior Medical Manager and MSL team Manger at Medical Nutricia Poland. Responsible for the implementing MSL role at Medical Nutricia building up MSL team and supervising team members during all aspects of the work.

Responsibilities: Targeting key opportunities in the medical community for Phase IV studies, advisory boards, consulting, and speaking, providing scientific updates to health care professionals. Supervising SAE reporting process and training company representatives, and members of market access, and marketing departments. Supporting Research Clinical Operation Department in selecting sites for studies as well as in educational activities dedicated to investigators, implementation, monitoring, and coordination Expanded Access ProgramResponsibilities: Targeting key opportunities in the medical community for Phase IV studies, advisory boards, consulting, and speaking, providing scientific updates to health care professionals. Supervising SAE reporting process and training company representatives, and members of market access, and marketing departments. Supporting Research Clinical Operation Department in selecting sites for studies as well as in educational activities dedicated to investigators, implementation, monitoring, and coordination Expanded Access Program

Responsibilities: supporting the Clinical Trials Research Associate team by documenting information concerning the progress of clinical trials. To help communicate actions between clients, international team members and others members of project team. To communicate with Ethic Committee and PIs, resolving problems at sites regarding Clinical Trials. Participating in a Monitoring Induction Plan (10 co-visits at sites with experienced CRA).Responsibilities: supporting the Clinical Trials Research Associate team by documenting information concerning the progress of clinical trials. To help communicate actions between clients, international team members and others members of project team. To communicate with Ethic Committee and PIs, resolving problems at sites regarding Clinical Trials.