Senior Director, Global Medical Affairs Molecule Lead, Sleep (Remote)

Jazz Pharmaceuticals
$222,400.00 - $333,600.00
vision insurance, 401(k)
United States, California, Palo Alto
Jul 11, 2025
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information. The Sr. Director, Global Medical Affairs Molecule Lead (GMAL), Neuroscience, Sleep will be the Medical Affairs leader for a molecule globally. As such, the position will require a deep understanding of the critical role of Medical Affairs as well as relevant clinical experience in the areas of neuroscience, sleep disorders and/or cardiovascular disease. The Sr. Director, GMA is a senior member of Jazz's Global Medical and Scientific Affairs (GMSA) organization, reporting directly to the Global Medical and Scientific Affairs, Therapy Area Head of Neurosciences. The Sr. Director, GMA will lead and be accountable for the development of the annual and long range Global Medical Plan, including an integrated evidence generation plan. He or she will ensure alignment of strategies and tactics to the Global Product Team and Franchise objectives. As such, this individual must embody strong medical leadership with communication skills, to effectively partner with both global and regional colleagues and counterparts across functions. The Sr. Director, GMA will lead the Medical Functional Matrix team for the molecule and be an active member of key cross-functional matrix core teams at Jazz (e.g., Global Product Team, Clinical Development Team). He or she will use their subject matter expertise to support molecule related decisions and provide a holistic overview of the GMA strategy for the molecule. Therefore, this individual must be highly collaborative and able to excel in global, cross-functional matrix team settings. Essential Functions Lead and develop the annual and long-range global medical tactical and evidence generation plans for the molecule. Able to harness insights to develop a holistic plan Lead the molecule Medical Functional Matrix Team (FMT) Lead and develop molecule data generation plans to support the Global Product Team and Franchise objectives. Work closely with GMSA Clinical Scientists, Real World Evidence Lead, and Global Value and Health Outcomes Research Lead to develop studies including the development of synopses, protocols and interpretation and execution of studies. Oversee the development of the disease and product scientific platform Craft product medical communication strategy and work closely with the Medical Communications Team to develop a publication plan Work closely with the Medical Communications Team to develop core medical materials (e.g., product and disease training, pivotal studies slide decks) to be disseminated and adapted by the regions Engage with Clinical Development Team to ensure important clinical evidence gaps are considered in the development program Work with Commercial Development Team to develop plans and materials to ensure successful product lifecycle Serve as the single global voice of Medical Affairs at key matrix teams. Considered as a subject matter expert in sleep disorders and/or cardiovascular disease and the therapeutic area. Maintain strong scientific knowledge of the relevant disease space and the competitive landscape Lead development of a high-quality integrated evidence generation plan Lead development of a differentiated Scientific Communication Platforms and Scientific Communication Guides Lead global external expert mapping efforts and provide input into regional external expert mapping Lead global external expert development and engagement plan Plan and lead scientific society interactions to identify partnership opportunities Plan and lead external expert and patient advisory boards Collaborate with Global Advocacy team to develop relationships with patient advocacy groups (PAG) and influencers to help develop the PAG engagement plan Develop the investigator sponsored trial/Collaborative study strategy Required Knowledge, Skills, and Abilities Clinical experience in sleep and/or cardiovascular disease required At least 7 years of experience working within medical affairs required Experience as a global medical director preferred Demonstrated track record of success in developing medical strategies that have a measurable impact Experience leading Phase 4 studies and supporting Real World Evidence/Health Outcomes Research required Experience with strategic and tactical planning for marketed product required; experience with both marketed and pipeline molecules preferred Experience leading cross-functional teams required Understanding of Regulatory and Commercialization frameworks, including reimbursement and market access required High degree of professionalism, integrity and collaboration required Exceptional verbal and written communication skills required Strong leadership, team building, negotiation and ability to execute required Results-oriented approach required to excel in fast-paced, high-growth environment Ability to travel required Required/Preferred Education and Licenses Doctorate degree required. MD (or equivalent) degree strongly preferred. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $222,400.00 - $333,600.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.