I have experience on Regulatory Writing  Writing clinical documents such as clinical study reports per ICH E3, protocols per ICH E6, patient information leaflets, patient safety narratives including the review process and quality control steps Academic Writing  Writing manuscripts and abstracts  Conducting comprehensive literature searches and performing critical analysis of clinical data  Reviewing slide decks for data integrity checks  Training modules Apart from this, I have also worked on clinical data mining, pharma company sites’ coverage for clinical data, journal’s coverage and clinical trial registry coverage....

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