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5.0 - 9.0 years
0 Lacs
hyderabad, telangana
On-site
Role Overview: You will provide expert support and functional and technical knowledge to ensure the scientific integrity and validity for clinical development, early development, and/or research projects. You will participate in the full lifecycle of producing key data and/or reports, including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities, and provide quantitative analytical support. Additionally, you will provide statistical support for regulatory submissions, planning, analysis, and reporting of clinical safety and efficacy summaries. You may also provide statistical support to research or othe...
Posted 1 week ago
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