30 March, 2022
1. Working knowledge of/experience with SAS/ R or any other business or research analytic software with an expertise in at least one type of software.
2. Statistical and numerical knowledge and expertise in analytic aspects.
3. Excellent interpersonal and communication skills.
4. Strong understanding of global clinical trial practices, procedures, methodologies.
5. Strong understanding of regulatory requirements for design, analysis and reporting of clinical trials
Education (minimum/desirable): MS/ MSc (in Statistics or equivalent) with 3+ years relevant work experience or PhD (in Statistics or equivalent) with 1+ years of work experience
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