PPfizer is looking for a motivated Aggregate Report Analyst with an international mindset to join the Worldwide Safety Department - Site of Milan. /ppbWhy Patients Need You /b /ppPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidence-based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. /ppbKey Experience Offer of this Role /b /ppThe Aggregate Report Analyst is a member of a structured team and will report to the Aggregate Report Team Lead, based in Milan. You will be placed in an international environment and interact with colleagues from different sites, mainly in Europe, United States, and Asia, with opportunities to expand your professional network. /ppbYou will have the opportunity to : /b /pulliBe a member of the Aggregate Report Center of Excellence team, collaborating with experienced colleagues worldwide. /liliLiaise with key partners, including Safety lines, QPPV, Regulatory, Medical, Clinical, Epidemiology, License Partners, and other stakeholders regarding document preparation and benefit-risk communication. /liliServe as the Worldwide Safety ‘point of contact’ for document issues for assigned products, if assigned by the manager. /liliIdentify process improvement areas and communicate solutions to management or relevant functions. /li /ulpbWe are happy to offer you : /b /pulliAn international team of junior and senior colleagues. /liliIn-depth training and mentoring. /liliA dynamic environment. /liliGrowth potential. /li /ulpbPrimary Responsibilities /b /ppYou will support and complete tasks following standard procedures, which may vary in scope and complexity, requiring flexibility and multitasking. You will also contribute to the team’s success through enthusiasm, collaboration, and your knowledge. /ppbYour main responsibilities will include : /b /pulliPreparing integrated safety data analyses for reports such as DSURs, PSURs, PBRERs, and other regulatory documents. /liliCommunicating safety resource and timeline needs, negotiating with project teams, and informing management. /liliEnsuring document production complies with SOPs and regulatory guidance, alerting management of deviations, and delivering documents on time. /liliOverseeing co-authors and understanding document dependencies across safety reports. /li /ulpWhat You Offer /ppbBasic Qualifications /b /pulliBachelor's in life sciences with 3+ years of relevant experience in safety, regulatory, or clinical fields. /liliFluency in written and spoken English; additional languages are a plus. /liliStrong scientific writing skills and data interpretation abilities. /liliAnalytical skills and familiarity with global regulatory guidance (ICH, FDA, EMA). /liliAlignment with Pfizer Values: Courage, Excellence, Equity, and Joy. /li /ulpbPreferred Qualifications /b /pulliAdvanced degrees (MD, DVM, PharmD, Master’s, or PhD). /liliExperience with data analysis software (Word, PowerPoint, Excel). /liliStatistical analysis proficiency and epidemiologic knowledge are desirable. /li /ulpYou are self-motivated, organized, and able to prioritize multiple projects. You possess good interpersonal skills, can influence and negotiate effectively, and are willing to mentor junior colleagues and external vendors. /p #J-18808-Ljbffr