ICBio as a Biometric Service provider, is expanding its wings as an International Clinical Research Service Provider.
Apply today for the below Positions
1) Clinical data management (CDM) 2) statistics (SAS Programmers) and 3) PV .
All 3 roles play a crucial role in clinical trials and in the drug development process – from trial design to protocol development. While CDM helps in generating high-quality, reliable, and statistically sound data from clinical trials, statistics can help improve protocol development, data analysis and clinical trial reporting. Pharmacovigilance represents all methods of detection, assessment, information and prevention of adverse drug reactions (ADRs) #
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