Schedule, finalize the agenda for, and attend all review meetingsEnsure comments obtained from review disciplines are captured in the electronic review and approval system, consolidated and communicatedCapture notes during live review meetings and review comments provided in offline review to ensure reviewer comments are appropriately reconciled and next steps are clearly communicatedTrack the review and evaluation of materials submitted and ensure approval status isdocumented for each reviewer prior to communicating finalization of the review processEnsure that content, quality, accuracy, and format of submissions comply with applicable internal policies and proceduresWork closely with Marketing and Medical Affairs to ensure that final pieces are consistent with the reviewer's recommendationsResponsible for electronic approval system (EAS) training (internal and external agencies) and processAdministrator of the EAS system for EU/RoWLiaise with marketing and medical teams and their agencies to address system/process questions, etc.Required Knowledge, Skills, and Abilities Bachelor's Degree with a minimum of three years of experience in the pharmaceutical or biotech industry requiredExperience associated with advertising and promotion regulations strongly desiredExtreme attention to detail with an ability to detect and correct errors/inconsistencies in various types of documentsExcellent verbal and written communication skillsMust be able to work successfully within a team/partnership environment and as an individual contributor, with a high level of professionalismAbility to interact effectively with all levels/roles of project team membersRequired/Preferred Education and LicensesPrior experience managing a review process using an electronic approval system (e.g.
Veeva)Jazz Pharmaceuticals is an Equal Opportunity Employer.