What we offer:
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Expertise in clinical trial programming, including data management and statistical analysis.
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Familiarity with regulatory requirements for clinical trials, such as FDA guidance documents, ICH guidelines, and CDISC standards.
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We work efficiently with large and complex datasets and are skilled in data cleaning, merging, and transformation.
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We have deep understanding of statistical methods and are capability of conducting complex statistical analyses.
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We provide accurate and reliable results, which are crucial for decision-making in drug development.
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We are skilled in adapting to changing project requirements and timelines and are able to work collaboratively with cross-functional teams and vendors including clinical operations, data management, statistics, Contract Research Organizations and outside laboratories.
- We can provide cost-effective solutions for data management and analysis. by developing efficient programming code, reducing the need for manual intervention, and providing quick turnaround time for deliverables.
