Experience

H1

• United States
• Software Development
• 300 - 400 Employee

• Senior Research Analyst

  • Sep 2021 - Present



SHORE INFOTECH INDIA PRIVATE LIMITED

• India
• 100 - 200 Employee

• Senior Research Analyst

  • Apr 2021 - Aug 2021



Cognizant

• United States
• IT Services and IT Consulting
• 700 & Above Employee

• Senior Process Executive

  • Aug 2019 - Dec 2020

  o Should originate agreements happening between pharma & healthcare companies across the globe through secondary research by going through company websites, stock exchanges, third party newswires etc.o Should be a self publishero Process agreements happening for commercial rights exchange for products/technologies between pharma & healthcare companieso Flexible with task rotation as per the team/SLA requiremento Clear TAT requests on daily basis and also should review all the closed requests raised to make updates in the database, if necessaryo Updating daily deals tracker, entity profiles tracker and origination tracker on time without errorso Gradually improve subject/process knowledge and improve decision making, contribute directly or indirectly to additional team task within given time lines



GD Research Center Pvt. Ltd.

• India
• Market Research
• 700 & Above Employee

• Research Analyst

  • Jun 2018 - Jul 2019

   Working on medical devices profiling through general secondary research in government sites, press releases and company product profile pages. To retrieve comprehensive information on the current clinical trials for specific condition, drugs, patient demographics, adverse events, study design or interventions currently under study. Tracking regulatory filings and analyze the regulatory information using data sources like SEC files, annual reports, FDA, EMEA & other regulatory websites, abstracts, journals, conferences & events. Maintaining the drugs datasets including drug class & MOA, developmental status, taxonomy for various therapeutic segments. Processing clinical trials to obtain clinical outcome data. Product profiling for a given drug product, determining patent status, drug approval history. Brand drug Analysis – Data mining of Clinical & Regulatory milestone/Development of product. Extensive secondary search on clinical trial from various registries and company sources