Ashwani Kumar

Senior Analyst/ Team lead:

Managed teams of 10+ employees and monitored projects to ensure progress

Coordinated team meetings to ensure goals were met and tasks were completed on time

Mentored and trained new team members to develop their skills and ensure successful performance

Developed and implemented new strategies to increase team productivity and customer satisfaction.

Process trainer for clinical trials to new hires, QC for the team members

Scheduled and assigned tasks to team members

Monitored performance and provided feedback.

Team’s MIS reporting

R&D Analyzer: Maintenance and enhancement of clinical and regulatory timelines (success rates/PTRS) of drugs through various sources like clinicaltrial.gov, EuDraCt, Drugs@FDA, press releases.
EMA, Ad-com calendars, companies websites, SEC filings, press release, annual reports, PubMed research articles and other sources available in public domain.
Drugs approval forecast and drugs phase progression probability.
Processing patent information from USPTO, Drug approvals from
Expertise into Ad-Hoc Pharma Projects.
In depth analysis of clinical trials. Product and indication addition from Clinical trials.
Clinical trial mapping, condition to indication mapping, sponsor mapping and daily CT import.

Competitive landscape research, Drug profiling

Daily media monitoring, and indication approval from FDA label change

New pharma companies coverage both private and listed, including company profile page and product portfolio, pipeline analysis.

Analysis of in-licensing, out-licensing deals, Merger & Acquisitions of top pharma companies.

Tier1 & 2 companies Pipeline validation annually

Processing patent information from USPTO, Drug approvals from USFDA and patent infringement/ Litigation cases and regulatory information.

Analyzing companies R&D pipeline, preliminary sales/quarterly reports, Annual reports, SEC filings.
Responsible for regular interactions with clients and collating, analyzing & reporting of business critical information required by organizations through word documents, excel, and powerpoint presentations.

At Genpact, have inculcated an extensive working experience as Associate in the health-care vertical, with BUPA Global (British United Provident Association).

Responsible for clinical investigation and processing of medical claims

Experienced in US Health-care, Knowledge of medical and health-care terminology, knowledge of US medical claims, experienced in US medical Claims of UHI (UHG) and GEOBLUE (BCBS) i.e TPA of BUPA in US.

Knowledge of ICD9, ICD10, CPT, HCPCS coding and medical billing