.**Work Schedule**Other**Environmental Conditions**OfficeAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.As a Senior Centralized Monitoring Analyst, you'll be supporting RBQM Strategy and centralized statistical and risk surveillance activities on assigned trials.**Summarized Purpose**:**Essential Functions**:- Serve as functional lead knowledgeable in RBQM methodologies, tools, processes, and central monitoring methods, tools, and systems.- Successfully influences study functional leads, with a focus on driving RBQM strategy, end to end data risk management and defining mitigations including proper monitoring strategy for critical-to-quality data and processes.- Ensures performance of assigned reviews with high quality, on-time results with more complex analyses or deeper root cause analyses to connect related signal to risks.- Provides training and guidance to junior team members.- Project leadership activities include: Leads the design and setup of study specific tools and centralized monitoring plan for data review; manages review timelines, develops analysis assignments for team, and supports budget management; organizes, communicateswith internal team, and delegates as appropriate to ensure reviews are completed on-time, on budget, with high quality; assists with report development, delivers reports, and leads centralized monitoring meetings; contributes to risk assessment through the completion of the department risk assessment tools. Participates in the cross-functional risk assessment review meetings and contributes to overall risk planning and monitoring strategy.- Specialist activities included focused efforts on the development of new tools and analyses within area of specialty.**Education and Experience**:Bachelor's degree or equivalent and relevant formal academic / vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years'). Prior experience in clinical monitoring, data management, biostatistics or related field in support of clinical trials is preferred