JOB SUMMARY 

The pipeline Medical Science Liaison (MSL) 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 in-house Clinical Site Monitoring (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 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, oncology early development (OED) and other affiliate medical department members to support AbbVie-led clinical trials.
  • Actively participate in cross-functional collaboration with Advocacy, Market Access, Health Economics and Outcomes Research, 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.
  • Liaise with Early Development, Search & Evaluation team, Discovery and/or Clinical Development to facilitate business and clinical development assessments and projects/programs.
• Relationship Management:
  • Provide scientific, business acumen and technical leadership to establish and maintain professional, credible relationships with investigators and thought leaders to facilitate potential research collaborations and educational efforts.
  • Act as the primary contact for investigator-initiated study ideas and support interactions with both local and global medical teams.
• Field Intelligence and Collaboration:
  • Collect and communicate field intelligence regarding competitive activities and investigator insights related to AbbVie’s clinical trials.
  • Maintain a high level of interaction with internal and external stakeholders to support scientific dialogue and promote AbbVie's strategic objectives.
  • Identify and communicate potential opportunities for partnering on new assets, unique treatment approaches, novel targets, etc.
• Regulatory and Compliance:
  • Ensure all activities are conducted in compliance with relevant laws, guidelines, and AbbVie’s policies.
  • Support physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, adhering to legal and regulatory requirements.
• Traveling is required, as per business needs