Requirements: English
Company: mAbxience
Region: Madrid , Community of Madrid
About the job
Position:
Medical Affairs Location: Madrid .
Want to know more?
The
Medical Affairs
is a strategic role within the Medical Department and serves as the
Internal Medical Expert (IME)
for
#mAbxience''s
biopharmaceutical portfolio, with a strong focus on
biosimilars 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 is
directly involved in the evaluation and selection of new molecules for the company pipeline , including the
clinical-scientific assessment of external assets in collaboration with KOLs , and the
co-creation of scientific strategies for product adoption and market access .
This position also plays a leading role in
scientific education , digital transformation of training content, and
engagement with external experts and partners .
The challenge!
Design and implement global medical affairs strategies for biosimilars and biologicals. Act as the
key medical-scientific partner
for internal teams and external stakeholders, including strategic commercial partners. Support the
selection and evaluation of candidate molecules and external assets , aligned with the companys R&D and commercial strategies. Ensure the
development and digitalization of scientific materials and training resources , adapted to a variety of stakeholder needs and channels. Lead the
scientific assessment and speaker selection
for specialized scientific seminars and educational events sponsored by the company. Strategic Expertise Maintain high-level, up-to-date expertise in biosimilars, monoclonal antibodies, and therapeutic areas of strategic relevance. Support World Wide company lounches across selected partners Provide 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 & Partnerships Serve as
primary medical liaison for strategic partners
post-launch. Build long-term scientific relationships with
KOLs, 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 Management Develop clear, accurate and engaging scientific content for diverse audiences. Lead or collaborate on the
digital transformation of medical and educational materials , ensuring effective use across e-learning platforms, virtual tools, and remote communication channels. Oversee the
creation, medical review and approval of training content , core slide decks, and partner-facing materials. Contribute to the
design and execution of scientific seminars and symposia , including
selection of external speakers , ensuring alignment with scientific rigor, therapeutic relevance, and company messaging. Publications and Evidence Generation Design and execute the
global 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 Collaboration Clinical Medical Advisors: Maintain close collaboration with Clinical Medical Advisors to obtain and interpret
clinical development data . These insights will support the
scientific validation of launch materials and training content
for 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 Compliance Operate within all applicable regulatory, legal, and ethical frameworks. Promote a culture of compliance