Job Description The Medical Science Liaison (MSL) - Gastroenterology serves to advance science and standards of care for patients through their engagement with healthcare professionals and other stakeholders within the healthcare system. Through scientific engagement, MSLs provide credible, practical and clinically relevant information and solutions to enable both the effective and safe use of AbbVie products. Collectively, as members of GMA, they work to make a remarkable impact on patient care around the world. MSLs work to communicate information and facilitate dialogue about AbbVie’s marketed products, and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice. This function is field based (NSW/QLD territory). Up to 80% of the time will be spent field-based. KEY DUTIES AND RESPONSIBILITIES Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts of strategic importance to AbbVie. Ensure a strong medical and scientific presence for AbbVie in key academic centres by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie. Serve as a point of contact within the Medical Affairs team for thought leaders and external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use. Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested. Attend relevant scientific meetings and conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives. Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements. Provide key thought leaders / external experts and internal medical, market access and clinical teams with scientific and technical support for publications of scientific or medical interest. Assist in the site selection, initiation, oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area of responsibility (e.g. post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorisation studies (phase IV). All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D SOPs. Act as the point of contact with thought leaders to facilitate investigator-initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate. Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Participate in the selection process to identify appropriately qualified thought leaders the company would wish to engage in collaborative efforts – such as potential research collaborations, or educational (e.g., congress, symposia) and advisory roles; while ensuring a high level of scientific or educational integrity in these collaborative efforts. Facilitate medical and scientific field intelligence – for example, competitor research and medical strategies, educational activities – and communicate, where appropriate, within the company, including cross-functional gap assessments. Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, company policies and accepted standards of best practice. Report any adverse event within 24 hours as per AbbVie’s policies and procedures. Proactively participate in AbbVie’s WHS programs, adhere to policies and promote a safe work environment at all times. Adhere to AbbVie’s internal codes of conduct and compliance processes. Other ad hoc duties such as administrative duties, as requested.