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Work ScheduleStandard (Mon-Fri)

Environmental ConditionsOfficeJob Description

Join Us as a Senior CM Analyst II – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance.As a

Senior CM Analyst II , you will identify and characterize issues and trends in operational and patient clinical trial data using analytical or statistical tools. You will leverage your operational experience and knowledge to evaluate issues and develop findings based on the data analyzed, communicating issues and potential risks to project team members for follow-up action.You will begin to develop a data analytics specialization and may execute data analytics lead tasks or function as the lead on projects.Clinical Trial Data Review & Analysis

Independently review and analyze clinical trial data using a variety of tools and systems in alignment with the centralized monitoring planFlex review assignments across the majority of different analysesCharacterize and track evidence of issues, signals,



and potential risksPerform complex analyses and root cause analyses to connect related signals to risksEnsure delivery of high-quality, on-time resultsRisk Identification & Monitoring

Participate in lead activities such as:

Contribution to the development of the Centralized Monitoring PlanDepartment risk assessment toolCross-functional risk assessment meetingsRisk reportsGenerating findings reports following review cycles

May function as the data analytics lead on some projectsCollaboration & Leadership

Communicate issues and potential risks to project team members for follow-up actionProvide training and guidance to junior team membersWork collaboratively across multidisciplinary teamsRequired:

Bachelor’s degree or equivalent and relevant formal academic/vocational qualificationExperience:

Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 5 yearsPrior experience in:

Clinical monitoringData managementBiostatisticsRelated field in support of clinical trials preferred

In some cases, an equivalency consisting of a combination of appropriate education, training,



and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.✅ Strong knowledge and skills while adhering to:Regulatory guidelinesGlobal SOPsClient expectations✅ Strong attention to detail and numerical skills✅ Strong analytical and problem-solving skills✅ Sound judgment and decision-making abilities✅ Ability to work productively with direct supervision✅ High level of confidentiality with clinical and proprietary client data✅ Demonstrated flexibility and adaptability✅ Ability to work independently and within a team environmentStrong computer proficiency with:

MS Office:

WordExcelPowerPoint

Interactive computer systemsAbility to:

Extract pertinent information from:

ProtocolsElectronic study data systemsStudy documentation

Identify trends in site/study data✅ Strong prioritization and workload management skills✅ Ability to adapt to changing project demands✅ Strong understanding of:Project protocolsProject documentationCentralized Monitoring PlansFunctional plansWork is performed in an office environment with exposure to electrical office equipmentOccasional drives to site locations with occasional travel both domestic and internationalWhen you join Thermo Fisher Scientific, you become part of a general team that values:PassionInnovationCommitment to scientific excellenceYou’ll work in an environment where collaboration and development are part of the everyday experience — and where your contributions truly make a difference.✨

Apply today to help us deliver tomorrow’s breakthroughs.

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📌 Sr CM Analyst II (Ciudad de México)
🏢 Thermo Fisher Scientific
📍 Ciudad de México