Head of the clinical research department in hematology

Head of the clinical research department, using his/her scientific and medical expertise, develops, coordinates and implements the opening of IRCCS clinical studies in coordination with health professionals, ensuring compliance with the regulations and deadlines.

He/she creates procedures specific to the field of hematology, defines the strategy for opening clinical trials, and ensures planning and validation of each study. He/she develops and maintains a network of professional partners and carries out regulatory and scientific monitoring, both at the national and international level.

The manager ensures compliance with Good Clinical Practices (GCP), particularly in terms of traceability and confidentiality. He/she supervises a team made up of project and study managers, clinical research assistants, laboratory technicians, and data managers, and coordinates relations with other partners involved.