.PPD, part of Thermo Fisher Scientific centralized monitoring group delivers a new approach to risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data. Centralized monitoring staff explores study data holistically to pinpoint meaningful signals, resulting in more efficient and effective issue resolution and a proactive approach to risk detection. Using this data-driven approach, PPD can address study problems or site performance quickly, directing remediation activities where needed and positioning on-site monitoring activity in a targeted approach.Centralized monitoring evaluates data within and across studies, sites, countries and regions. Our analytic approach provides insight into:- Data errors, deviations- Trends, outliers- Unusual variation (or lack of variation)- Potential data manipulation, fraud- Other systematic errors or data integrity issues.As a Senior Centralized Monitoring Analyst, you'll be supporting centralized statistical and risk surveillance activities on assigned trials.At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.Summarized Purpose:Essential Functions:- 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.- May participate in a project lead or development specialist role, or a combination of both.- 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.- 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 qualification- Previous 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