**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** At Thermo Fisher Scientific Inc., our mission is to make the world healthier, cleaner, and safer. As a Sr CM Analyst I, you will play a pivotal role in advancing global health initiatives through world-class clinical research. Our collaborative environment, dedication to excellence, and brand-new resources will empower you to excel and make a global impact. Centralized Monitoring (CM) is an integral part of PPD’s risk-based quality management (RBQM) strategy. We deliver 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. Ongoing data assessments from our Centralized Monitoring group facilitates dynamic adaptation of monitoring plans with a focus on critical-to-quality risks that drive data quality and have the greatest impact on data integrity and subject safety. **Job Responsibilities** · Serve as the Centralized Monitoring functional lead, with knowledge in RBQM methodologies, tools, and processes. · Lead activities such as developing centralized monitoring plans and generating findings reports. · Manage review timelines and support budget management. · Serve as functional representative, communicating and working with the study team. · Ensure reviews are complete, generate reports, and lead Centralized Monitoring Review meetings to discuss issues and risks with the study team. · Contribute to risk assessment through department risk assessment tools and participate in cross-functional risk assessment review meetings. · Characterize and track evidence of issues, signals, and potential risks. · Provide training and mentorship to junior team members. **Education and Experience** · Bachelor's degree or equivalent relevant formal academic/vocational qualification. · At least 5 years of experience in clinical monitoring, data management, biostatistics, or a related field in support of clinical trials. · Equivalent combinations of education, training, and/or directly related experience will be considered. **Knowledge, Skills and Abilities** · Strong organizational skills with adherence to regulatory guidelines and global SOPs. · Outstanding attention to detail and numerical skills. · Proven analytical and problem-solving abilities. · Ability to work independently and within a team environment. · Solid oral and written communication skills. · Proficiency with MS Office and interactive computer systems. · Ability to extract pertinent information from standard study documentation. **Working Environment** Thermo Fisher Scientific values the health and well-being of our employees and encourages a balanced environment. You must be able to: · Communicate effectively with diverse groups. · Work upright, stationary, and/or standing for typical working hours. · Lift and move objects up to 25 pounds. · Work in non-traditional environments. · Use and learn standard office equipment and technology proficiently. · Perform under pressure while prioritizing multiple projects. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.