Ikram B.

Coordination and monitoring of clinical studies (multicenter, interventional, and observational). Patient coordination and scheduling. Active participation in innovative pharmaceutical trials. Rigorous data collection, verification, and entry into eCRFs. Medical device management: installation, maintenance, traceability, and compliance. Quality control and data consistency in eCRFs. Writing procedures for uniform data entry in compliance with protocols. Ensuring adherence to Good Clinical Practices (GCP) and protocols.

Supervision of the quality of meal services for patients: compliance with specifications, traceability. Implementation of the risk analysis and critical control point (HACCP) system and the Sanitary Control Plan (PMS). Management of non-conformities: implementation of CAPA (Corrective and Preventive Actions). Management and continuous training of a team of 30 employees. Elaboration and monitoring of budget + forecasts. 30% reduction in occupational safety and health risks through updating the ERVP and targeted corrective actions. Monitoring of workplace accidents, improvement of floor safety and risk areas.

Performing intravenous blood draws and sample preparation (centrifugation, blood smears). Hematological analyses: CBC, blood typing, sedimentation rate. Maintenance, calibration, and use of laboratory instruments. Administrative management of laboratory activities.