Pipeline Medical Science Liaison

About this role

Therapeutic area: NEURO/EYE CARE/PSYCHIATRY/OBESITY This position covers operations across the entire country. Preferred candidates' locations: Central Poland (Warszawa, Łódź), candidates based elsewhere will also be considered. The pipeline Medical Science Liaison (pMSL) is a field-based scientific expert dedicated to facilitating scientific dialogue and supporting the scientific, clinical and business objectives of a designated therapeutic area, with a strong focus on clinical research and enterprise critical studies globally.

The MSL role embodies our unified R&D approach by fostering seamless collaboration with local Clinical Site Management (CSM) teams, especially Clinical Research Associates (CRAs). This integrated approach ensures the alignment of scientific vision and operational execution, enhancing the efficiency and effectiveness of pipeline development and acceleration. The role emphasizes strong engagement with investigators, healthcare professionals, and key scientific institutions to elevate AbbVie's scientific credibility and support clinical research and development of investigational products and compounds.

The MSL serves as a conduit of information to a cross functional External Experts (EE) regarding AbbVie’s investigational products, and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, code of conduct, AbbVie’s policies and procedures and accepted standards of best practice. Key Responsibilities: Scientific Expertise and Communication: Ensure a strong medical and scientific presence for AbbVie in investigational sites and key scientific centers.

Serve as a scientific expert within designated therapeutic areas, facilitating the effective communication of AbbVie's scientific information. Deliver credible presentations on scientific matters and AbbVie’s pipeline to clinical investigators and stakeholders. Clinical Trial and Cross-Functional Support: Engage with clinical trial sites to Understand enrollment and screening barriers and work with the site to find potential solutions/mitigation strategies.

Collaborate closely with CSM, CDO, Clinical Development and other affiliate medical department members to support AbbVie-led clinical trials. Actively participate in cross-functional collaboration with Medical Managers, Medical Advisors, Market Access, Health Economics and other relevant teams to integrate scientific insights into AbbVie's pipeline development programs. Participate in country and site feasibility and selection process to help identify qualified EE to participate in AbbVie clinical program and to collaborate with Medical Affairs activities such as advisory boards, steering committees, congresses, symposia, etc.