Requirements: English
Company: mAbxience
Region: Madrid , Community of Madrid
About the jobPosition:Medical AffairsLocation: Madrid .Want to know more?TheMedical Affairsis a strategic role within the Medical Department and serves as theInternal Medical Expert (IME)for#mAbxience'sbiopharmaceutical portfolio, with a strong focus onbiosimilars and monoclonal antibodies. This individual is the main medical liaison internally and externally, responsible for the scientific accuracy, clinical value, and strategic communication of all medical data throughout the product lifecycle.In addition to traditional medical affairs responsibilities, this role isdirectly involved in the evaluation and selection of new molecules for the company pipeline, including theclinical-scientific assessment of external assets in collaboration with KOLs, and theco-creation of scientific strategies for product adoption and market access .This position also plays a leading role inscientific education, digital transformation of training content, andengagement with external experts and partners .The challenge!Design and implement global medical affairs strategies for biosimilars and biologicals.Act as thekey medical-scientific partnerfor internal teams and external stakeholders, including strategic commercial partners.Support theselection and evaluation of candidate molecules and external assets, aligned with the companys RD and commercial strategies.Ensure thedevelopment and digitalization of scientific materials and training resources, adapted to a variety of stakeholder needs and channels.Lead thescientific assessment and speaker selectionfor specialized scientific seminars and educational events sponsored by the company.Strategic ExpertiseMaintain high-level, up-to-date expertise in biosimilars, monoclonal antibodies, and therapeutic areas of strategic relevance.Support World Wide company lounches across selected partnersProvide medical input into pipeline decisions, guiding molecule selection processes based on clinical need and scientific evidence.Drive the early-stage assessment of external assets for the comnay in collaboration with KOLs and internal stakeholders.Stakeholder Engagement PartnershipsServe asprimary medical liaison for strategic partnerspost-launch.Build long-term scientific relationships withKOLs, investigators, scientific societies, and patient advocacy groups .Engage with stakeholders to identify scientific needs and develop targeted education and communication strategies.Scientific Communication, Digital Training Speaker ManagementDevelop clear, accurate and engaging scientific content for diverse audiences.Lead or collaborate on thedigital transformation of medical and educational materials, ensuring effective use across e-learning platforms, virtual tools, and remote communication channels.Oversee thecreation, medical review and approval of training content, core slide decks, and partner-facing materials.Contribute to thedesign and execution of scientific seminars and symposia, includingselection of external speakers, ensuring alignment with scientific rigor, therapeutic relevance, and company messaging.Publications and Evidence GenerationDesign and execute theglobal publications plan, targeting key congresses and journals.Ensure that scientific communication reflects the totality of clinical evidence and supports regulatory and market access goals.Collaborate on post-marketing studies and real-world evidence generation (Phase IV, NIS).Cross-functional CollaborationClinical Medical Advisors:Maintain close collaboration with Clinical Medical Advisors to obtain and interpretclinical development data. These insights will support thescientific validation of launch materials and training contentfor external stakeholders, especially partners.Marketing Commercial:Review and validate marketing materials; provide strategic and scientific input to support global brand positioning and value messaging.Regulatory Affairs:Support the regulatory team in preparing and reviewing medical sections of SmPCs, patient information leaflets, and global dossiers.Pharmacovigilance:Contribute to safety data interpretation and communication; escalate safety-relevant information in compliance with SOPs and applicable regulations.Business Development:Assist in evaluating external opportunities and licensing discussions by contributing clinical and scientific expertise.Quality Assurance:Ensure all activities align with GCP, regulatory guidelines, and internal quality standards.Ethics and ComplianceOperate within all applicable regulatory, legal, and ethical frameworks.Promote a culture of compliance, integrity, and ethical conduct within and beyond the team.Escalate compliance or scientific integrity concerns in a timely and appropriate manner.What do you need?Education:Degree in Health Sciences (e.G. Medicine, Pharmacy, Biology). Advanced degree (PhD, MSc) or specialization in relevant fields is highly desirable.Languages:Fluent in Spanish and English (both written and spoken).Experience:At