Medical Affairs

mAbxience; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading biopharmaceutical company in Madrid seeks a Medical Affairs expert to oversee strategic communication and scientific accuracy for their biosimilars portfolio. The role involves collaboration with KOLs, training development, and scientific education to enhance product adoption and market access.

Servicios

Benefits and Savings Club

Training and language learning platform

Wellness platform with unlimited free psychologist sessions

Development plans, internal mobility policy

Formación

• At least 2 years in Medical Affairs, clinical research, or scientific communication roles.
• Experience in training, digital content development and KOL engagement preferred.

Responsabilidades

• Design and implement global medical affairs strategies for biosimilars.
• Serve as primary medical liaison for strategic partners post-launch.
• Develop clear, accurate and engaging scientific content for diverse audiences.

Conocimientos

Communication

Project Management

Critical Thinking

Educación

Degree in Health Sciences

PhD or MSc

Descripción del empleo

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 company’s 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.
• 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, 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 least 2 years in Medical Affairs, clinical research, or scientific communication roles.
• Experience in training, digital content development and KOL engagement preferred.
• Strong understanding of monoclonal antibodies and biosimilars.
• Skills :
• Outstanding communication and presentation abilities
• Strong scientific and critical thinking skills
• Project management and organizational discipline
• Open mindset for innovation and cross-cultural collaboration
• Travel : Willingness to travel nationally and internationally as required

Competences :

• Strategic and analytical thinking
• Exceptional verbal and written communication (Spanish / English)
• Scientific writing and educational storytelling
• Digital literacy for training and communication tools
• Strong interpersonal and stakeholder management skills
• Team collaboration and leadership
• Adaptability and resilience
• Integrity and compliance orientation

KPIs

• Scientific accuracy and quality of launch and training materials
• Partner satisfaction with medical support and training
• Timeliness and relevance of scientific communication
• Engagement levels in educational activities
• Execution and impact of the publications plan
• KOL relationships and feedback
• Contribution to pipeline and asset evaluation decisions
• Flexible start time from Monday to Friday (full-time).
• Benefits and Savings Club.
• Training and language learning platform
• Wellness platform with unlimited free psychologist sessions
• Development plans, internal mobility policy.

What will the Selection process be like? ️

Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels.

Prepare well! We will continue with an in-person / virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test.

Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process.

Do you think this offer is not for you?

COMMITMENT TO EQUAL OPPORTUNITIES

Our group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3 / 2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Seniority level

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Mid-Senior level

Employment type

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Full-time

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