Senior Regulatory Information Management Associate.
Overview: Jazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing and commercializing meaningful products that address unmet medical needs. We are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. Our therapeutic areas of focus include sleep and hematology/oncology – areas in which we have a deep understanding of the patient journey and a suite of products and product candidates to address critical needs. We are looking for the best and brightest talent to join our team. If you’re looking to be a part of a company with an unwavering commitment to improving patients’ lives and being a great place to work, we hope you’ll explore our career openings and get to know Jazz Pharmaceuticals. Responsibilities: The Senior Associate, Global Regulatory Operations, Regulatory Information Management (RIM), provides Global Regulatory Affairs support for Jazz’s RIM system (Veeva Vault RIM). This position will work closely Global Regulatory Affairs, as well as other functions within R&D including IT, Clinical, Medical Writing, Nonclinical, CMC, and Quality to support training, documentation, user experience, and maintenance of the RIM system and acts as a champion for the broader Global Regulatory team and its use of the RIM system. Responsibilities : Support for RIM users across R&D, working to leverage optimal value for Jazz from the Veeva Vault RIM suite of products (Registrations, Submissions and Submissions Archive applications) Develop training material and contribute to user communications including newsletters and intranet page Support business related queries, by providing appropriate how-to guidance and advice Provide data requests from users across GRA and R&D contributing groups, through the use of Veeva Vault RIM reporting f...