The Manager of Global Medical Affairs, Independent Medical Education (IME) Grants will be responsible for the successful development and management of the global medical education grant program for assigned therapeutic areas (Tas). The position will support delivery of impactful medical education that enhances patient care by improving Healthcare Professionals' ability to

Excellent working knowledge on pharmacovigilance and drug safety regulations (ICH, GxP) Work to streamline and optimize business processes based on industry best practices. Generate listings from the safety database, both standard reports and ad hoc queries. Conduct peer review of safety database queries for accuracy and completeness of the results. Coordinate safety syst

may require a work schedule that may include working outside of "normal" work hours, to meet business demands. Occasional public contact requiring appropriate business apparel. 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

The Director, Toxicology is accountable for managing the global nonclinical regulatory and investigative toxicology of assigned Jazz portfolio products, and likewise to support his/her reports overseeing those products. They will collaborate with their direct reports and other members of the toxicology group, Early Development non clinical scientists, and members of Jazz

The Integrated Data Analytics and Statistical Programming Group (IDASP) within the Department of Data sciences is responsible for developing software for the analysis of clinical study data in accordance with departmental SOPs and guidelines. Essential Functions Attend multi disciplinary team meetings, representing the programming function. Create or review and approve pr

Develop and implement regulatory strategies to facilitate the progress of programs in all phases of development Serve as the Regulatory Affairs representative on project teams; assure the progress of projects by providing direction, solutions, and feedback to the teams Lead regulatory interactions with health authorities, marketing partners, and vendors for their products

Develop and lead the execution of strategic roadmap and objectives for the clinical data platform(s) Partner cross functionally to optimize Jazz's use of the clinical data platform(s) and develop/implement change management strategies to maximize adoption Provide vision, motivation, leadership, and mentoring to the Clinical Data Innovation team. Plan, hire and adapt resou

Facilitates the design, development, production and delivery of Global Clinical Development Operations (GCDO) digital systems in order to achieve operational excellence, optimize data quality and realize efficiencies wherever possible Represents their department and collaborates with Information Services (IS), Clinical Operations, Outsourcing, Medical Writing, Clinical Da