Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
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 I, 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.
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Independently review and analyze clinical trial data using a variety of tools and systems in alignment with the centralized monitoring plan
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Flex review assignments across the majority of different analyses
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Characterize and track evidence of issues, signals, and potential risks
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Perform complex analyses and root cause analyses to connect related signals to risks
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Ensure delivery of high-quality, on-time results
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Participate in lead activities such as:
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Contribution to the development of the Centralized Monitoring Plan
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Department risk assessment tool
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Cross-functional risk assessment meetings
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Risk reports
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Generating findings reports following review cycles
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May function as the data analytics lead on some projects
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Communicate issues and potential risks to project team members for follow-up action
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Provide training and guidance to junior team members
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Work collaboratively across multidisciplinary teams
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Bachelor’s degree or equivalent and relevant formal academic/vocational qualification
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Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 5 years
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Prior experience in:
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Clinical monitoring
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Data management
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Biostatistics
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Related 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:
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Regulatory guidelines
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Global SOPs
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Client 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 environment
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MS Office:
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Interactive computer systems
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Extract pertinent information from:
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Protocols
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Electronic study data systems
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Study documentation
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Identify trends in site/study data
✅ Strong prioritization and workload management skills
✅ Ability to adapt to changing project demands
✅ Strong understanding of:
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Project protocols
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Project documentation
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Centralized Monitoring Plans
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Functional plans
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Work is performed in an office environment with exposure to electrical office equipment
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Occasional drives to site locations with occasional travel both domestic and international
When you join Thermo Fisher Scientific, you become part of a global team that values:
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Passion
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Innovation
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Commitment to scientific excellence
You’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.
