Aggregate Report Analyst

Pfizer is looking for a motivated Aggregate Report Analyst with an international mindset to join the Worldwide Safety Department - Site of Milan. Why Patients Need You Pfizer 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. Key Experience Offer of this Role The 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. You will have the opportunity to : Be a member of the Aggregate Report Center of Excellence team, collaborating with experienced colleagues worldwide. Liaise with key partners, including Safety lines, QPPV, Regulatory, Medical, Clinical, Epidemiology, License Partners, and other stakeholders regarding document preparation and benefit-risk communication. Serve as the Worldwide Safety ‘point of contact’ for document issues for assigned products, if assigned by the manager. Identify process improvement areas and communicate solutions to management or relevant functions. We are happy to offer you : An international team of junior and senior colleagues. In-depth training and mentoring. A dynamic environment. Growth potential. Primary Responsibilities You 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. Your main responsibilities will include : Preparing integrated safety data analyses for reports such as DSURs, PSURs, PBRERs, and other regulatory documents. Communicating safety resource and timeline needs, negotiating with project teams, and informing management. Ensuring document production complies with SOPs and regulatory guidance, alerting management of deviations, and delivering documents on time. Overseeing co-authors and understanding document dependencies across safety reports. What You Offer Basic Qualifications Bachelor's in life sciences with 3 years of relevant experience in safety, regulatory, or clinical fields. Fluency in written and spoken English; additional languages are a plus. Strong scientific writing skills and data interpretation abilities. Analytical skills and familiarity with global regulatory guidance (ICH, FDA, EMA). Alignment with Pfizer Values: Courage, Excellence, Equity, and Joy. Preferred Qualifications Advanced degrees (MD, DVM, PharmD, Master’s, or PhD). Experience with data analysis software (Word, PowerPoint, Excel). Statistical analysis proficiency and epidemiologic knowledge are desirable. You 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. J-18808-Ljbffr

Location: Milano, Lombardia, IT

Posted Date: 8/17/2025