Debika Das

Background

About Debika Das

Currently I am working as Drug safety specialist at PAREXEL International and holding 7+ years of experience in Pharmacovigilance in case processing programs with multiple clinical trial and post-marketing programs from India. I have been worked on multiple safety databases including ARISg (7.4) and Argus (7.0). In addition to Safety databases, I have equally got exposure for exploring Electronic Data captures (EDCs) and RAVE. • Knowledge of US and ICH safety reporting regulations and guidelines. • Good knowledge in monitoring and tracking Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. • Processed fatal, serious, non-serious cases in ARGUS and ARISG • Good knowledge in Literature search for adverse drug reactions related to drugs. • Proficient in data entry and drug safety database. • Excellent written and verbal communication skills. • Good interpersonal, organizational skills and analytic thinking. • Demonstrated ability to work with MS Office products such as Word, Excel, Access and Powerpoint. Specialties: Pharmacovigilance and Clinical Research.