Pipeline Medical Science Liaison

• Facilitate scientific dialogue and support scientific, clinical, and business objectives in the designated therapeutic area
• Serve as a field-based scientific expert focused on clinical research and enterprise-critical studies globally
• Collaborate with Clinical Site Management teams, especially Clinical Research Associates, to align scientific vision and operational execution
• Engage investigators, healthcare professionals, and key scientific institutions to support clinical research and development of investigational products and compounds
• Provide scientific information about AbbVie’s investigational products and compounds in development in a strictly scientific, non-promotional manner
• Maintain a strong medical and scientific presence at investigational sites and key scientific centers
• Deliver credible presentations on scientific matters and AbbVie’s pipeline
• Engage clinical trial sites to understand enrollment and screening barriers and develop mitigation strategies
• Collaborate with CSM, CDO, Clinical Development, Medical Managers, Medical Advisors, Market Access, Health Economics, and other relevant teams
• Participate in country and site feasibility and selection processes
• Identify qualified external experts for AbbVie clinical programs
• Collaborate on Medical Affairs activities including advisory boards, steering committees, congresses, and symposia
• Establish and maintain professional relationships with investigators and thought leaders
• Act as the primary contact for investigator-initiated study ideas
• Collect and communicate field intelligence regarding competitive activities and investigator insights
• Identify opportunities for partnering on new assets, treatment approaches, and novel targets
• Ensure all activities comply with applicable laws, guidelines, and AbbVie policies

• Advanced degree in health sciences or clinical discipline required (e.g., PharmD, MD, PhD or MSc)
• Candidates with an undergraduate degree and significant relevant experience may be considered
• Minimum 1-2 years relevant experience in medical affairs, clinical research, or a similar role
• Demonstrated expertise in the aligned therapeutic area, scientific methods, clinical research and development, and current regulatory requirements
• Excellent communication and presentation skills, with proficiency in scientific storytelling
• Demonstrated ability to develop and maintain strong collaborative relationships
• Demonstrated ability to work independently and as part of a cross-functional team and in a matrix environment
• Fluent in Polish and English
• Strong commitment to compliance with relevant rules and procedures, and to scientific quality and integrity

• Equal opportunity employer
• Commitment to operating with integrity, driving innovation, transforming lives and serving the community