Milva Monova

Background

About Milva Monova

Clinical Project Management Professional managing global clinical studies and programs including risk-based monitoring trials, and project teams. Leading all aspects of a study from operational strategy development and start up to close out. Has been involved in global study management across Europe, Africa, North America, Asia Pacific, Latin America and Phases II & Biotech trials leadership experience. Responsibilities include customer primary key contact, budget and finance management, study document management, risk management, as well as the management and coordination of the following service lines: Clinical Monitoring, Site Management, Medical Monitoring, Regulatory Affairs, Data Management, Biostatistics & Programming, Medical Writing, Safety and Third Party Vendors. Significant experience in managing Japan-conducted clinical trials. Demonstrated competencies and experience leading autoimmune disease (Rheumatoid Arthritis, Lupus) trials, women's health trials, neurodegenerative diseases, as well as rare disease (Fabry and Pompe) trials and programs. Experienced Key Customer Account Manager and cross-cultural communicator.