Summary
Overview
Work History
Education
Skills
Accomplishments
Interests
Work Availability
Quote
Timeline
Generic

TEJASWINI RACHURU

Market Analyst
Hyderabad,India

Summary

A thorough passionate who craves for interesting and diversified roles at every given walk of life. I bring in excellent academic background rich experience in various pharmacological classes of drugs of various therapeutic areas, clinical trial phases, new drug discovery and development process.

Overview

4
4
years of professional experience
6
6
years of post-secondary education

Work History

Market Analyst

Medsphere India Pvt Ltd
Goregaon, Maharashtra
08.2021 - Current
  • Focused on doing primary and secondary research for CI across various therapeutic area landscapes including CKD and COVID-19
  • Responsible for doing analysis of Press releases, Clinical Trials and Publications on weekly basis
  • To represent content analysis through PowerPoint presentations and Newsletters based on Client's requirement
  • To represent marketing strategies of competitors in dashboard format, pie and bullseye charts, etc.
  • To keep track on daily CT updates and additions, regulatory approvals and market launches
  • Being trained on conducting KOL interviews
  • To be able to handle multiple tasks based on deliverables
  • Attracted new clients by creating and implementing innovative marketing strategies
  • Streamline analysis for efficiency and accuracy

Associate Content Analyst Clarivate

Analytics
Hyderabad, India
12.2019 - Current
  • To update information about progress of drug, from early-stage research to approval and launch in Cortellis – a competitive intelligence product that provides insights in data through a suite of life science intelligence solutions.
  • Perform literature reviews including retrieval and analysis of data, study design terms, competitive product pipeline information, epidemiology trends, treatment patterns etc.
  • Document review: Study and analyze the presentations and various research works on drugs.
  • Review the documents related to clinical development of drugs.
  • Handling & solving the client queries.
  • Expertise in Literature search from regulatory portal and other scientific database sources.
  • Study and analyze the presentations from different conferences such as ASCO, EAACI, EHA, etc.
  • And various research works on drugs.
  • Write and edit articles and content in the product specifically in the field of immune-oncology and gene therapies.
  • Quality Assurance : Achieve and maintain consistent quality standards.
  • Perform quality-check of drugs updated by peers and vendors.
  • Ensure that all work is complete and of high quality prior to shipment to client.

Junior Researcher

Cognizant Technology Solutions
Hyderabad, India
01.2018 - 11.2019
  • Gather and analyze data for clinical trials.
  • Generate final summary reports based on data collected from clinical trials.
  • Review the documents related to clinical development of drugs.
  • Review safety and AE profiles, scientific endpoints, and clinical outcomes of patients from charts and figures from different clinical source documents.
  • Writing and reviewing the clinical trial results postings and results framing.
  • Maintain databases, queries, and reports; perform data entry and check reviews.
  • Track progress of clinical studies, ensuring projects meet timelines and quality expectations.
  • Responsible for framing results and reporting outcomes of clinical trials.
  • Review of clinical trial information from regulatory labels and supporting documentation.
  • Generate final summary reports based on data collected from clinical trials.
  • Streamlined research processes to meet tight deadlines for multiple projects

Education

Bachelors of Pharmacy -

Bharat School of Pharmacy
Ibrahimpatnam, TS
01.2013 - 01.2017

Intermediate -

Sri Gayatri Junior College
Habsiguda, Hyderabad
01.2011 - 01.2013

Skills

    Data analysis

undefined

Accomplishments

  • Analytical method development and validation of Triperidol and Fentanyl citrate in bulk and pharmaceutical dosage form by RP- HPLC.”A new, simple, fast, rapid, accurate, efficient, and reproducible RP-HPLC method for the simultaneous analysis of Droperidol and Fentanyl citrate was developed, and it was validated according to the ICH guidelines.
  • VOLUNTEER EXPERIENCE: Saksham world sight day-Volunteered for Saksham World Sight Day Book Editing Drive”, which is a part of CST initiative - To convert various books from PDF to WORD to help the visually impaired.

Interests

Dance

Music

Travel

Arts

Work Availability

monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
swipe to browse

Quote

The way to get started is to quit talking and begin doing.
Walt Disney

Timeline

Market Analyst

Medsphere India Pvt Ltd
08.2021 - Current

Associate Content Analyst Clarivate

Analytics
12.2019 - Current

Junior Researcher

Cognizant Technology Solutions
01.2018 - 11.2019

Bachelors of Pharmacy -

Bharat School of Pharmacy
01.2013 - 01.2017

Intermediate -

Sri Gayatri Junior College
01.2011 - 01.2013
TEJASWINI RACHURUMarket Analyst