• Proactively identify key regional healthcare decision makers (HCDMs) • Serve as the primary medical liaison between AbbVie and the HCDM • Build strong relationships to understand customer needs • Facilitate generation of real-world evidence (RWE) consistent with approved therapeutic area medical planning • Participate across assigned therapeutic area and healthcare landscape strategic committees • Customize communication of scientific, health outcomes, and health policy information to HCDMs and influencers • Document and communicate meaningful observations which lead to insights on a regular basis • Identify relevant emerging scientific, health economic, and health policy trends • Primary interface and initial point of contact for small-scale, RWE opportunities with regional level HCDMs • Anticipate, identify and address population-level scientific, outcomes research, and health policy needs of customers • Facilitate scientific exchange between AbbVie Medical Leadership and accounts • Maintain and enhance clinical, scientific, and healthcare landscape expertise • Participate in various therapeutic advisory activities involving marketed and investigational products

• Serve as the primary interface with clinical trial sites, collaborating with Clinical Development and Operations to ensure high-quality study execution, specifically clinical trial enrollment. • Participate in planning and setup for your region, aligning with local colleagues and CROs. • Develop deep expertise in multiple therapeutic areas, including inflammatory bowel disease. • Act as the regional subject matter expert and credible scientific leader. • Build and maintain relationships with opinion leaders, clinical investigators, and study staff within your region. • Provide scientific support to Clinical Development, Medical Affairs, Commercial, and other teams. • Support activities such as local, regional, national, and as needed, international, congresses, share clinical and scientific insights with cross-functional teams. • Operate ethically and comply with all laws, regulations, and policies.

Role Description The Medical Science Liaison (MSL) position serves as the primary field-based scientific expert for Jazz Pharmaceuticals' products. The MSL will establish and maintain scientific and clinical relationships with medical professionals, researchers, and other members of the scientific community in the therapeutic area of Sleep Medicine/Neuroscience. This is a field-based position covering California and Hawaii and requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence. Essential Functions/Responsibilities - Provide field-based scientific exchange and communication of FDA approved and pipeline products. - In support of FDA approved products, work within the Medical Science Liaison team’s objectives. - Identify, establish, and maintain scientific relationships with opinion leaders regarding disease-state and product-specific information. - Facilitate scientific development of pipeline compounds at research centers, and secure the company’s presence in the designated therapeutic areas. - Support the clinical operations organization, as needed, in Jazz Pharmaceuticals sponsored research. - Serve as primary liaison with investigators interested in developing and performing investigator initiated research. - Cross-functional nature of role requires close alignment with the Medical Affairs, Commercial, and Clinical Development groups. - Document and forward reports of adverse events according to Jazz’s policy to ensure safe and effective use of Jazz Pharmaceuticals' products. - Attend and provide scientific support of Medical Affairs activities and scientific sessions at regional and national congress meetings. - Develop and prioritize solutions to problems, understand relationship between actions and results, and appreciate needs of customers. - Proactively seeks out and demonstrates successful peer coaching of other team members. - Successfully manages at least two large cross-functional projects with demonstrated leadership and collaboration skills while successfully maintaining geographical responsibilities. Qualifications - Ability to effectively communicate scientific data to both internal and external customers, including opinion leaders and managed care organizations. - Knowledge of geography and key opinion leaders preferred. - Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel. - Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest. - Collaborative, team-based approach; ability to network and partner with internal and external stakeholders, including commercial and R&D partners, medical opinion leaders, academic institutions, large group practices, managed care organizations, medical directors, and pharmacy directors in institutional practices. - Ability to work evenings and weekends. - Ability and willingness to travel 60% of work days. - Valid driver’s license and live within 60 miles of a major airport. Requirements - An advanced doctorate degree (PharmD, MD, DO, PhD or equivalent). - A minimum of 0-2 years of experience in the pharmaceutical industry and/or clinical/research experience (MSL experience preferred). - Preference will be given to those with experience in Sleep Medicine; however, experience in Neurology, Psychiatry or other relevant backgrounds will be considered. Benefits - Medical, dental and vision insurance. - 401k retirement savings plan. - Flexible paid vacation. - Eligibility for a discretionary annual cash bonus or incentive compensation. - Discretionary equity grants in accordance with Jazz’s Long Term Equity Incentive Plan.

• Communicate new and other important approved medical content to targeted health care professionals (HCPs) • Provide externally truthful, accurate and scientifically supported information in response to unsolicited medical requests from HCPs and other stakeholders • Provide internally product and indication expertise for any Seqirus/CSL colleague • Deliver presentations to relevant stakeholders in accordance with the designated medical strategy established by the Spanish, European and Global Medical Affairs team • Facilitate communication between HCPs and HCOs, any healthcare decision maker and Medical Affairs colleagues • Facilitate both Seqirus sponsored clinical trials, collaborative research, and investigator initiated research activities • Facilitate and support Medical Affairs contribution to awareness and education of all stakeholders in close collaboration with internal functions • Search actively for customer insights that contribute to the development of product medical strategies