•Authored and reviewed protocol registrations, result registrations to be disclosed on Clinicaltrials.gov, clinicaltrialsregister.eu (EudraCT)•Performed CSR synopsis and Protocol maintenance and amendment tasks for Clinicaltrials.gov•Authored clinical trials results summary for National Registry of Health Research (ReNIS) of Argentina•Analysis of clinical study reports, protocols, statistical analysis plan, and table listing figures (TLFs) to prepare protocol registration, results registration forms and results summaries •Performed redaction of clinical trial documents (including Clinical Study Reports, Protocol and Statistical Analysis Plan) including voluntary redaction as per sponsor specific QC checklist, redaction as per EMA policy 0070 and per Health Canada guidelines•Worked on web-based data entry system PRS to register a clinical study or submit results information for a registered study, EudraC The European database for all interventional clinical trials on medicinal products authorized in the EEA•Worked on PharmaCM a clinical trial disclosure platform used to manage the complex process of authoring, reviewing, editing, approving and publishing clinical trial application and disclosure data•Worked on Trialassure a clinical trial disclosures and transparency reporting software•Hands on experience of working on database and systems including Medidata Clinical Trial Management System (CTMS), Electronic Regulatory Information System (ERIS), Eclipse, Intralinks, Secure Shell (SSH) File Transfer Protocol (SFTP) Server, Amazon WorkSpace (AWS)•Sound knowledge of Clinical trials, Good Clinical Practices, ICH guidelines, recent updates on National Institutes of Health (NIH) guidelines required for ClinicalTrials.gov.

Worked as assistant professor, provided lectures of Organic chemistry, analytical chemistry and Physical chemistry along with practical. I was involved in administrative tasks along with academics.