
10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 B2B
Biotechnology • Science • B2B
Danaher Corporation is a leading global life sciences and diagnostics innovator that develops and supplies instruments, technologies, software, and services to accelerate scientific research, biotechnology development, and clinical diagnostics. The company operates through businesses focused on biotechnology tools, diagnostics platforms, and life sciences products, leveraging the Danaher Business System and an acquisition-driven strategy to scale technologies and support customers across academia, pharmaceutical and biotech companies, and clinical laboratories.
🔥 16 hours ago
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10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 B2B
Biotechnology • Science • B2B
Danaher Corporation is a leading global life sciences and diagnostics innovator that develops and supplies instruments, technologies, software, and services to accelerate scientific research, biotechnology development, and clinical diagnostics. The company operates through businesses focused on biotechnology tools, diagnostics platforms, and life sciences products, leveraging the Danaher Business System and an acquisition-driven strategy to scale technologies and support customers across academia, pharmaceutical and biotech companies, and clinical laboratories.
• Responsible for all activities of clinical trial data management including CRF design, database and edit check development • Plan and implement the data management portions of clinical research projects • Develop systems for organizing data to analyze, identify and report trends • Work with clinical leads, CRAs and statistical department to provide accurate data acquisition • Responsible for timely identification of problems or issues that could affect the results or timely completion of the trial • Provide data management portions of clinical study reports, and participates in report review
• Bachelor's or master's degree in science or health care area • 5+ years of experience in developing and executing clinical data management procedures • Experience in in-vitro diagnostics (IVD), Pathology, and Companion Diagnostics clinical research preferred • Excellent organizational skills • Proficient with Microsoft Access and Excel • Good understanding of medical terminology, human physiology and laboratory testing preferred
• Paid time off • Medical/dental/vision insurance • 401(k)
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