ph3About us /h3pChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here. /ph3Air and Care Franchise /h3pWithin the three Business Units ( Discover more here ), Air and Care Franchises are responsible for the development and implementation of the Therapeutic Area Strategies. Each Franchise is organized by stage of development with fully empowered and enhanced teams of: Pipeline Development Team - focused on delivering innovation and programs leadership accountabilities in close collaboration with RD, Commercial Portfolio Management Team - focused on maximizing the vantaggi for the patients and the full potential of marketed / close-to-launch assets, including Life Cycle Management strategies. /ppAir and Care Franchises are also supported by the Global Medical Affairs and Global Value Access functions. /ph3Who we are looking for /h3pThis is what you will do /ppThe Global Publication Lead is responsible for defining and executing the global publication strategy and tactical publication plan for all global studies or all studies run by affiliates with a global impact, included in the Global Integrated Evidence Generation Plans (iEGPs). /ppThe role ensures timely, compliant, and impactful dissemination of scientific data through international congress presentations and international peer reviewed publications, aligned with the overall medical and commercial strategy of the products at global level and for the prioritized geographies. /ppYou will be responsible for /ph3Key Duties and Responsibilities /h3ulliPublication Strategy PlanningulliDefine the overall global publication strategy across the Evidence Generation Plan in alignment with Global Medical Affairs and product strategies /liliDevelop and maintain global integrated publication plans for each study run by global functions as part of IEGP including subanalyses, post hoc analyses, pooled data analyses etc of studies conducted by GMA or Global Clinical Development /liliPrioritize data dissemination opportunities based on:



Scientific value and novelty of data; Product lifecycle stage; Medical and commercial strategic needs; Geographic relevance and priorities /li /ul /liliCongress Abstract StrategyulliIdentify and recommend target international scientific congresses and coordinates affiliates activity in terms of targeting national congresses with “anchor” abstracts /liliOversee global abstract planning, submission timelines, and approvals /liliCoordinate with internal and external stakeholders to ensure scientific consistency and strategic positioning of congress deliverables /li /ul /liliManuscript Journal StrategyulliDefine manuscript strategy for each study, including:ulliPrimary, secondary, and exploratory publications /liliTarget international journals (tiered approach based on impact factor, audience, and geography) /liliRecommend appropriate international journals depending on the data and strategic objectives and geographical scope /li /ul /liliOversee the writing, review, submission, revision, and publication process for manuscripts /liliManage relationships with external medical writers and publication vendors, where applicable /li /ul /liliThe person will:ulliwork in close partnership with Global Evidence Generation and medical leads / managers, Global Clinical Development functions (incl. Statistics and data managers), GVA team, global commercial team /liliensure alignment between publication plans and Evidence Generation priorities, medical strategies, product and indication strategies, geographic scope and priorities /liliact as the central publication point of contact for EGP related studies /liliensure all publication activities comply with company policies and SOPs, GPP (Good Publication Practice) guidelines, authorship and disclosure requirements, regulatory and ethical standards, will support and follow the approval workflows /lilimonitor progress, timelines, and deliverables across all EGP publications /li /ul /liliYou will need to haveulliAdvanced degree preferred: MD, PhD, PharmD, or MSc in life sciences or a related field. /lili2+ years of experience in similar role in pharmaceutical companies. /liliStrong knowledge of scientific congress landscape, peer reviewed journals, publication ethics and compliance standards /liliStrong strategic thinking with the ability to translate data into impactful publication plans. /liliExcellent understanding of clinical development and evidence generation. /liliAbility to balance scientific rigor with strategic business needs.



/liliStrong stakeholder management and cross‑functional collaboration skills. /liliProject management capability with excellent attention to detail and timelines. /liliFluent in English (oral and written communication) /li /ul /liliWe would prefer for you to haveulliExperience working in Global Medical Affairs functions /liliExposure to respiratory area /li /ul /li /ulh3Location /h3pThe role can be based in the HQ in Italy or in one of Chiesi affiliates in Europe /ph3Compensation Range (package applied for role based in Italy) /h3pThe minimum salary for this role is €67.120, aligned to our established salary framework. The final offer will reflect the candidate’s skills, experience, qualifications and internal equity considerations. /ppThis role is eligible to participate in an annual bonus scheme, subject to company and individual performance. /ppIn addition, we offer a comprehensive benefits package including pension, private medical insurance, wellbeing programme, flexible benefits programme. /ppThe package outlined above is based on the role being located in Italy. Where the role is offered in a different country, the applicable salary, bonus and benefits will be aligned to the relevant local market and internal frameworks. Full details of the applicable package will be provided at the appropriate stage of the recruitment process. /ph3What we offer /h3pNo matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way. /ppWe provide top-class benefits, including comprehensive healthcare programs, work-life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive. /ppChiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination. /p /p #J-18808-Ljbffr

📌 Global Publication Lead, Medical Affairs (Parma, IT)
🏢 Biopharma Careers
📍 Parma