Medical Affairs Support Expert HUB

Role:

Medical Affairs Support Expert HUB

Short Role Description / Purpose 
Support the activities of the Medical Affairs-Primary & Specialty Care Department 

Long Description

• Support the Medical Affairs Department, in compliance with ethical, deontological and legal rules as well as internal company procedures, in the management of the scientific training of all internal staff, of foreign partners and in the management of onboarding and scientific training of the External Operational Force (FOE);
• Represent the operational reference point for scientific training and education activities for the Medical Affairs Department;
• Develop scientific training presentations, insights, newsletters in order to ensure correct and effective scientific information to the FOE, internal staff and partners;
• Develop correct and referenced scientific exchange presentations and materials for Medical Affairs interactions with HCPs;
• Represent the operational reference point for Medical Information activities at national and international level;
• Manage Medical Information requests from an operational point of view, for complex bibliographic searches and answers to medical-scientific questions;
• Support the Medical Affairs Department in compliance with ethical, deontological and legal regulations as well as internal company procedures, in the development of scientific projects, where required;
• In agreement with the Head and the Medical Affairs HQ team, provide support in scientific presentations and insights in inter-company contexts;
• Provide support in the generation of new data and publications in the therapeutic areas of reference;
• Support the Drug Safety & Regulatory Affairs function from a scientific medical point of view, where required, eg. in the scientific review of pharmacovigilance documentation and registration dossiers;
• Support the Medical Affairs and Marketing team in the preparation of promotional materials, ensuring the correctness and ethics of the scientific information contained therein on the basis of current regulations and in compliance with the deadlines defined;
• Provide support in the evaluation, through the company tools and in compliance with the Group's policies, of the company scientific materials used so that they are consistent with the scientific evidence and the lines of development of the therapeutic area;
• Support the review / drafting of company procedures and policies relating to the Primary & Specialty Care Business Unit;
• Know the legal, deontological and corporate rules governing the activities within their competence, and act in compliance with them.
• Maintain updated clinical, scientific and technical expertise in Company’s therapeutic areas. 
• Supports international partners in medical-scientific activities related to the Primary Care portfolio;

Education
•    Scientific University degree (Pharmacy, Biology, Chemistry, or similar) 
 

Further  Requirements 
•    Fluency in English and Italian – written and spoken;

•    Knowledge of pharmaceutical regulations; 
•    High concern for quality;
•    Strong computer skills, including MS Office (Excel, Power Point) and IOS systems.