Medical Advisor Autoimmunity

Description

Summary: This physician role drives clinical study design and execution, provides medical expertise across cross-functional teams, and contributes to medical strategy in autoimmunity. Highlights: 1. Central role in clinical development and medical strategy 2. High level of independence with strong organizational impact 3. Engage with key opinion leaders and scientific experts **Work Schedule** Standard (Mon\-Fri)**Environmental Conditions** Office**Job Description** **Job Description – Medical Advisor Autoimmunity** **About Thermo Fisher Scientific** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our mission is to enable our customers to make the world healthier, cleaner and safer. We foster a collaborative, respectful and flexible work environment in a global setting. **Location** : remote Spain, London, Paris, Upsala **Position Summary** The Medical Advisor Autoimmunity is a physician who plays a central role in clinical development and medical strategy across the portfolio. This role drives clinical study design and supports execution, contributing to development decisions and providing medical expertise across cross\-functional teams. The position operates with a high level of independence and has strong impact across the organization, supporting multiple functions including R\&D, Clinical Affairs, Regulatory, Marketing, PLCM and Quality Assurance. **Key Responsibilities** **Clinical Development \& Study Design** * Drive clinical study design and support execution for new and existing assays * Define clinical strategy, endpoints, and study objectives in collaboration with Clinical Affairs and R\&D * Act as a core team member in product development projects **Medical Strategy \& Product Development** * Provide medical input into development of new assets and intended uses * Contribute to shaping portfolio direction based on clinical relevance and patient needs **Clinical Approval Board (CAB)** * Actively participate in the Clinical Approval Board (CAB), the internal governance forum where investigator\-initiated studies and collaborations are reviewed and approved * Contribute to scientific and medical evaluation of proposals and support decision\-making **Post\-Market Surveillance \& Risk Assessment** * Lead medical evaluation of product performance, complaints, and clinical risks * Contribute to benefit\-risk assessment and safety\-related decisions * Ensure medical consistency across post\-market activities **Cross\-Functional Collaboration** * Partner closely with Clinical Affairs, R\&D, Regulatory, Marketing, PLCM and Quality Assurance teams * Provide medical input to support product development, regulatory activities and commercialization **External Engagement** * Engage with key opinion leaders and scientific experts * Represent the company at scientific meetings and congresses * Contribute to scientific discussions and external collaborations **Basic Qualifications** * MD required * Clinical background with experience in autoimmunity, immunology, rheumatology or related areas such as neurology, gastroenterology or general medicine preferred **Skills \& Competencies** * Strong clinical judgment and ability to translate science into decisions * Ability to work independently and drive initiatives * Demonstrated ability to adapt to new tools and technologies, with a required mindset to effectively leverage AI and digital solutions * Excellent communication and stakeholder management skills * High proficiency in English (required); additional European languages (e.g., German, Swedish) are a plus **Additional Information** * Reporting line: Global Medical Director, Autoimmunity * Location: Europe * Travel: up to 25% worldwide