Medical Advisor Gastroenterology

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ph3Company Description /h3 pAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. /p h3Job Description /h3 pWe are seeking a bMedical Advisor /b in the bGastroenterology /b therapeutic area — a passionate and driven professional who is eager to make an impact and join our dynamic team. /p pIn this role, you will have the opportunity to contribute to our medical strategy and work closely with key stakeholders, reporting directly to the Medical Lead. /p pMain responsibilities include: /p ol liTo warrant the medical know-how of the Affiliate regarding the relevant therapeutic areas of assigned products (including AbbVie products, competitors and general knowledge of specific diseases). /li liTo drive Medical activities to support the Brand Strategy and integrate it into the Brand Plan /li liTo represent the Italian Affiliate in the relevant therapeutic Corporate Medical Development setting. /li liTo prepare the medical plan of activities for each product of the relevant area, on an annual basis and to update it as appropriate. /li liTo contribute to the design and improvement of AbbVie Medical Department Italy (AMDI) systems and processes (e.g. AMDI SOPs and Guidelines) with the aim of ensuring best practice as well as compliance to all applicable regulations and Company procedures. /li liTo undergo training relevant to the function and to be familiar and updated with the AbbVie local and international procedures relevant to the Job Description. /li /ol pAdditional responsibilities: /p ol liTo manage the budget of the relevant therapeutic area (including local clinical studies) as approved in the medical plan. /li liTo be responsible for: ol liThe design of local AMDI clinical studies. /li liThe review, approval,



fulfillment of contract agreements of Investigator Initiated Studies (IISs). /li /ol /li liTo foster the participation of the Affiliate to International clinical trials and provide the Medical Lead/Head Medical Affairs/Affiliate Medical Director and Research and Development with appropriate comments regarding the design and implementation of International protocols. /li liTo identify potential sites for carrying out International and local clinical studies and maintain a liaison with them throughout the study conduct in cooperation with Clinical Research Department. /li liTo maintain a continuous relationship with Key thought Leaders and External Expert as to the relevant therapeutic area. /li liTo address queries by physicians regarding the relevant products (including medical support on marketed products to the Pharmacovigilance Unit). /li liTo design or participate to the design of AbbVie events (e.g. Satellite Symposia), warranting an appropriate medical support to the Commercial Divisions and in agreement with the International and local SOPs. /li liTo provide medical-scientific update on TA, products and competitors, as agreed with the Commercial Divisions and to provide medical training when requested/necessary. /li liTo review promotional material before the approval of the Head Scientific Service, warranting the appropriateness of its medical content and the independence of assessment. /li liTo review the Summary of Product Characteristics and Insert Leaflets, prepared by Regulatory Affairs, before final approval of the Head Scientific Service, as to products of the relevant therapeutic area. /li liTo support the Scientific Training Specialist(s)



of the relevant Medical Affairs Unit in preparing the annual scientific training plan for the sales force and its delivery, including the preparation of product handbook(s). /li liTo provide medical support to the Pharmacovigilance Unit as to AEs reported in clinical trials on the relevant products. /li /ol h3Qualifications /h3 ul liMedical bdegree strongly preferred /b, or Italian equivalent to Laurea Magistrale in life science/chemistry related topics. /li liMinimum of 3 years’ working experience in clinical context or in pharmaceutical/biotechnological industry, in a scientific/medical role, within cross functional teams /li libExperience in gastroenterology therapeutic area /b /li liAbility to transform strategies into feasible and realistic actions /li liAbility in leading, motivating, and coordinating cross functional team /li liExcellent knowledge of the health sector and of its development /li liEffective management of the work in a matrix structure /li liKnowledge of financial principles and processes /li liFluency in written and oral English (Minimum Common European Framework Level: C1). /li /ul pPreferred: /p ul liMedical Specialization, PHD in medical sciences /li liProven success in pharmaceutical/biotechnological context /li /ul h3Additional Information /h3 pYour total reward package at AbbVie will be made up of multiple components, including compensation, well-being and benefits.br/In this role, you will receive base pay and annual short term incentive subject to AbbVie's global policy. You will also receive a number of benefits including life assurance, medical plan, flexible benefits, etc. /p pIn this role, you will also be entitled to receive a company car. /p pFull details of our comprehensive package will be shared during the recruitment process. /p pThe national collective bargaining agreement applicable to this position is B011 – CCNL Chemical-Pharmaceuticals Industry. /p pAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. /p /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7bhdtg