Thermo Fisher Scientific
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
CM Analyst I
November 4
Thermo Fisher Scientific
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
Description
• Analyze operational and patient clinical trial data using analytical or statistical tools. • Review clinical trial data using a variety of tools and systems in alignment with the centralized monitoring plan. • Characterize and track evidence of issues, signals, and potential risks. • Ensure results of reviews are appropriately recorded according to department procedures. • May participate in the development of risk characterization and reporting. • Support review set-up, including updating department databases and pulling reports.
Requirements
• Bachelor's degree or equivalent experience in a relevant academic or vocational field. • Previous clinical trial experience (2+ years) in clinical monitoring, data management, biostatistics, or a related field supporting clinical trials. • Strong attention to detail and numerical skills. • Good analytical and problem-solving skills with sound judgment in decision-making. • Ability to maintain confidentiality with clinical and proprietary data. • Flexibility, adaptability, and capability to work both independently and within a team environment. • Proficiency in MS Office (Word, Excel, PowerPoint) and capacity to learn and use interactive computer systems. • Ability to extract pertinent information from standard study documentation and identify trending site/study data. • Strong oral and written communication skills in English. • Good understanding of project protocols, documentation, and medical terminology. • Broad working knowledge of the roles, functions and processes of conducting clinical trials.
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