Simone Betti Email & Phone Number

Tuscany, Italy

Responsible for the Medical education plans from strategic concept development through implementation and execution. Responsible for the development of the International Medical Education Strategy and education design, development, and deployment of programs.Responsible for establishing effective collaborations with Academic Institutions, Medical.

Tuscany, Italy

• Key Tasks and Responsibilities
• Leverage scientific and clinical knowledge to engage customer, scientific exchange in areas of strategic focus at Lilly.
• Identification and development of potential solutions to address scientific customer needs.
• Strategic analysis, planning and prioritization to maximize efficiency
• Ability to build mutually beneficial two-way dialogue with SE
• Deep understanding of customers’ needs, in order to deliver best in class customer… Show more Key Tasks and Responsibilities

Tuscany, Italy

• Guarantee the regulatory agency's requirements on pharmacovigilance, in order to maintain the Products Marketing Authorization.
• Ensure compliance with the Regulatory internal and external requirements.
• Responsible for managing, coaching and developing the people of the team.
• Qualified Person for the Italian Regulatory Authorities.

Italy

Enable scientific exchange between Lilly and the scientific community to address important medical and scientific questions to improve patient outcomes

Tuscany, Italy

Contributes to the achievement of the Business Unit Objectives, through the management and scientific coordination of promotional activities and promotional messages; improve the effectiveness of scientific communications through cross-functional activity with the different functions: marketing and medical

Florence, Italy Metropolitan Area

• Provide adequate scientific documentation to answer questions or clarifications of the internal and external customers.Collaborate with Marketing for the development and implementation of communication strategy..
• Responsible for searching, selecting and analyzing the scientific literature for preparing a reimbursement dossier for Regulatory… Show more Provide adequate scientific documentation to answer questions or.
• Responsible for searching, selecting and analyzing the scientific literature for preparing a reimbursement dossier for Regulatory Agency.
• Scientific intelligence vs main competitors. Show less

Florence, Italy Metropolitan Area

• Evaluate, re-elaborate and manage Adverse Events occurring during the Clinical Trials and Spontaneous Reactions reported by Local Health Units, Healthcare Professionals and private individuals.
• Manage the communications to the Regulatory Agency regarding Pharmacovigilance Topics.
• Analyzed the main Pharmacovigilance Signals from the PhV Database

Tuscany, Italy

Development of the Periodic Product Quality Evaluation, which collects all the information to evaluate the quality of the product and the production process in a defined period. This Documentation is mandatory to maintain the authorization to produce drugs by regulatory agencies

Diploma Di Master Universitario Di I Livello In Farmacovigilanza E Discipline Regolatorie, Farmacovigilanza

Master in Farmacovigilanza e Discipline Regolatorie

Università Degli Studi Di Firenze, Laura In Chimica E Tecnologie Farmaceutiche

Maturità Tecnica, Diploma Di Scuola Superiore

Chemistry Ad Pharmaceutical Technologies