Presentación
The Global Medical Affairs Manager is a core member of of the Medical Affairs Team and represents the nexus of cutting-edge medical and scientific insights with internal and external stakeholders contributing to drive medical innovation in the therapeutic areas of competence and throughout the entire product life cycle with a strategic mindset and vision. Reporting to the Global Medical Affairs Lead, he/she is in charge for active and value-adding scientific contributions to cross-functional teams internally and engagement with key external stakeholders Therapeutics area: cardiovascular and Respiratory&Pain&Allergy
Organización
You will work at a prominent Italian pharmaceutical company with a global presence and a solid track record of over 130 years in the industry, located in Badalona. With a team of more than 700 professionals in Spain, they are among the top 15 pharmaceutical companies in the country. Their current focus covers key areas such as cardiovascular risk, respiratory, analgesia, male sexual health, and the digestive system. Additionally, they are committed to research and development of new products in various therapeutic areas, including oncology.
Función
Main Activities & Responsibilities Serve as the primary scientific and medical expert for the assigned therapeutic area/products with internal and external stakeholders. Participate as representative of Global Medical Affairs in Global Project Teams/Global Brand Team. Contribute with a strategic mindset to the development and execution of the Global Medical Affairs Plan according to strategic company milestones and budget.Work closely with internal stakeholders to execute that all activities in the Medical Affairs plan designed to meet shared objectives are implemented and performed in a timely manner. Contribute to marketing strategies with scientific input and collaborate on organizing medical events. Provide impactful feedback/information to internal stakeholders on emerging clinical and scientific trends from external interactions to help shape company research and to ensure the safe and appropriate use of Menarini Group products. Build specific excellence and integrity within the healthcare community. Develop contacts with key clinicians, patient’s association and other medical/scientific groups. Contribute to Mapping of Key Opinion Leaders (KOLs) on the disease and KOLs insights on the product, worldwide. Analyze, synthesize, and present medical scientific information in a structured way. Prepare and deliver training sessions on therapeutic areas and assigned products. Assist in the development and execution of clinically relevant medical meetings (e.g., advisory boards, consultancy and investigator meetings), as requested. Contribute to planning, coordination, and presentations at global and national advisory boards and other meetings. contribute to publication planning, delivery, and dissemination Contribute to the development and implementation of key international congresses Develop, review and approve responses to unsolicited requests for medical information in line with company’s SOPs and code of practice. Develops, review and approve promotional and educational materials for the allocated therapeutic area. Act as Study Medical Expert in the development of studies from initiation until publication and evaluate initiated investigator studies in the correspondent therapeutic area. Interact with key medical societies Support and review of grants for scientific projects in collaboration with clinical operations Provides support and input into regulatory authority interactions, for example RMPs, PSURs,defending risk/benefit, Product Information Provides support and input into early phase or market access aspects of clinical development plans. Contribute to developing SOPs and Working Instructions to improve efficiency, quality and compliance in processes.Coordinate approval of contracts for external (consultancy/speaker) activities with HCPs or otherthird parties. Collaborate with external providers in different activities according to the Menarini Groupcode of practice and policies. Ensure all medical projects, materials and presentations are compliant to pharmaceutical codes. Act within compliance and legal requirements as well as within company guidelines. Other duties as assigned
Requisitos
Job Requirements Education (preferred: Medical Doctor Degree) Years of experience (≥2 ) Language skills and level of proficiency (Business fluency in English, both spoken and written) Good verbal and written communication skills. Strong organizational, and cross-functional collaboration skills. Driven by Learning and Personal Development Ability to effectively collaborate in a dynamic and global environment.
Oferta
What We Offer A visible and strategic role within a growing global function. Opportunity to work closely with senior leaders and cross-functional experts across Clinical Science, BD&L, and Operations. Professional development through exposure to high-impact, strategic projects. A collaborative, mission-driven culture focused on innovation and patient outcomes. Flexibility to work from various European locations (hybrid options available). How to Apply Interested in this opportunity? Here’s what to do: 1. Speak with your HR Business Partner and/ or line manager (in accordance with local policy) to align on your interest. 2. Send your CV to Jana Loumova (see contact details above) by 28th November 2025. 3. For any questions, feel free to contact HR/Talent Acquisition or the hiring manager directly. This is your chance to take the next step in your Menarini journey. Join a team that’s shaping the company’s future and driving strategic growth.