Job Details
Director, Global Medical and Promotional Regulatory Affairs
2025-07-03 Jazz Pharmaceuticals all cities,CAIf 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 totransform the lives of patients and their families. We are dedicated to developinglife-changing medicines for people with serious diseases— often with limited or notherapeutic options. We have a diverse portfolio of marketed medicines, including leadingtherapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments.Our patient-focused and science-driven approach powers pioneering research and developmentadvancements across our robust pipeline of innovative therapeutics in oncology andneuroscience. Jazz is headquartered in Dublin, Ireland with research and developmentlaboratories, manufacturing facilities and employees in multiple countries committed toserving patients worldwide. Please visitwww.jazzpharmaceuticals.comfor more information.
The Director, Global Medical and Promotional Regulatory Affairs will be a member of Jazz Pharmaceuticals' Global Medical and Promotional Regulatory Affairs group and will be assuming a leadership role in the promotional materials review; will be responsible for directing the regulatory aspects of internal and external communications, including advertising and promotional activities in the US; will provide insight, judgment and sound decisions on promotional and non-promotional programs and tactics for assigned products in oncology or assigned therapeutic area. The Director works autonomously and collaboratively with Regulatory, Medical, Legal/Compliance and Commercial organizations. The individual develops and applies expertise to ensure promotional programs and tactics are compliant with regulations and company policies while supporting the achievement of business objectives.
Essential Job Functions:
Lead the promotional material review committee (PMRC) for assigned products/therapeutic areas in the US for Jazz Pharmaceuticals.
Provides input on decisionsregardingconcepts and draft promotional materials to satisfy the letter and spirit of FDA promotional regulations, corporate standards and policies and business objectives
Presents clear position statement and risk analysisto leaders in the regulatory department, medical affairs and other departments as needed
Serve as the Promotional Regulatory Affairs lead for a new product launch through contributions to the US Core launch team for assigned product in oncology.
Provide regulatory advice, andsupport to the organization.
Lead the PMRC process and manage regulatory aspects of the review and approval for product promotional materials,maintaincompliance of promotional materials with the governing FDA regulations, andsubmitpromotional materials to the Office of Prescription Drug Promotion (OPDP) ina timelyfashion.
Effectively partner with Regulatory colleagues, Medical Affairs, Legal/Compliance,Marketingand other departments as needed to ensure the thorough,timelyand efficient review of all materials
Exercise independent leadership skills and regulatory subject matter expertise
Work closely with thePromotional Regulatory Affairs leadand other team members to develop regulatory subject matterexpertiseand leadership skills
Provide regulatory support for Medical Affairs Review Committee (MARC)
Contribute to the development of regulatory strategy through assigned Global Regulatory team
Lead interactions with FDA/OPDP for assigned product(s) including submission of materials for advisory comments for full approval and accelerated approval products.
Further develop depth and current awareness of evolving FDA regulations and interpretations, FDA advisory comments, enforcement letters and policy issues affecting the pharmaceutical/biologics industry. Interprets and communicates FDA perspective to relevant stakeholders and recommends policy and/or process changes as needed, consulting with Regulatory colleagues as appropriate
Required/Preferred Education and Licenses:
B.S or B.A. degree in a scientific discipline or equivalent (a non-scientific degree with industry experience tocomplimentthe degree).
Advanced degree in a scientific discipline (e.g.PharmD)stronglypreferred.
Substantial pharmaceutical industry experience with proven experience in regulatory affairs advertising and promotion
Experience with Oncology and new product launch support is strongly preferred
Strong understanding of FDA regulations and guidelines
Strong judgment and decision-makingskills
Excellent collaboration, verbaland written communication skills
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: $188,800.00 - $283,200.00
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: