Experience

LARVOL

• United States
• IT Services and IT Consulting
• 100 - 200 Employee

• Team Lead

  • Dec 2021 - Present

  Analyzes, visualizes and interprets data from multiple sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences, annual meetings etc, • Great knowledge of Oncology Therapeutic Area (solid and liquid tumors)• Great knowledge of biomarker preclinical studies, all development phases (1 to IV) and FDA events, Monitor upcoming cancer milestones via secondary research• Daily monitoring news for top tumour types from multiple sources.• Knowledge of targeted therapies and MOAs• Produce comprehensive and robust secondary researches, excellent attention to detail and demonstration of resourcefulness through work• Able to do multi-task and work with evolving time-sensitive deadlines and priorities • Strong analytical abilities and QC skill• Highly proficient in the use of MS word, PowerPoint and Excel• Database quality checks/assurance • Able to make PPT and contributes to high-quality presentation materials • Able to do presentation for strategic company profile in front of management • Maintain daily as well as weekly work tracker of team• Handled team queries• Delegate tasks and set deadlines • Oversee day-to-day operation• Monitor team performance via spot check and report on metrics• Able to provide new strategy for coverage of new task• Discover training needs and provide training• Recognize high performance and reward accomplishments• Suggest and organize team building activities• Able to attend all type of calls via team or Zoom app• Excellent communication and leadership skills Show less

• Research Analyst-Oncology Biomarker

  • Jan 2020 - Dec 2021

  • Data Analysis, Data Mining & Secondary Research • Carry out and supervise secondary market research in diverse domains and identify emerging trends• Strong analytical and decision making skills as per available data• Great knowledge of biomarker and personalized medicine• Ability to track data related to biomarker and drugs associations• Great biomarker analysis from all publication either from pubmed, conferences etc• Able to analyze biomarker association either sensitive or resistant on the basis of publication result• Able to do competitive analysis of the drugs related to biomarker area for oncology• Effectively and proactively communicate with team members and management• Strong mentor and QC skill• Competitive scientific meetings and literature coverage• Supervising, mentoring, training and management of juniors within the team • Database quality checks/assurance • Bio-pharmaceutical company coverage, analysis, making PPT, and presentation skills• Collect & analyze the information from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences, annual meetings (ASH, ASCO), Etc.• Handled conferences coverage• Handled Daily surveillance for top tumor types• Handled all request like regimen addition, alterations and drug addition with respective team• Good computer skills and skilled with Ms word, Ms PowerPoint, MS Excel, and Outlook• Able to quickly acquire working knowledge regarding a variety of scientific/medical fields• Strong interpersonal skills and the ability to be flexible in varying environment Roles & Responsibilities Show less



ADI Group

• India
• IT Services and IT Consulting
• 1 - 100 Employee

• Research Analyst

  • Jun 2015 - Dec 2019

  Roles & Responsibilities • Carry out and supervise secondary market research in diverse domains and identify emerging trends • Collect and analyze the data related to diverse sector • Strong analytical and decision making skills as per available data • Able to do competitive analysis of the drugs • Able to write CSR as per ICH E3 guideline • Peer-review of TFLs and able to create Tables from listing and figures as per client requirement • Patients safety narrative (PSN) • Data integrity (DI) check • Academic writing like literature review through comprehensive searches in the PubMed and Google scholar and research article as per client requirement • Write references as per MLA, APA, Chicago, Harvard, and Vancouver style • Able to write articles and blogs-medical niche • Effectively and proactively communicate with team members and management • Able to generate effective tables and graphs and use of applicable Microsoft software • Give Training related to clinical trials (Phases, Drugs, Therapeutic areas, Clinical trial design, Accrual of the study etc) and searching technique to medical writing team members. • Meet project deadline always • Do quality check of the automatically scrapped conferences in the Confowiz software. Analysis of correct molecules/drugs/biomarkers/receptors/technology drugs/clinical trials in the conferences’ database • Great mentoring skills • Good computer skills and skilled with Ms word, Ms PowerPoint, MS Excel, and Outlook • Able to quickly acquire working knowledge regarding a variety of scientific/medical fields • Good knowledge of drug development process • Strong interpersonal skills and the ability to be flexible in varying environment Roles & Responsibilities Show less



Citeline-TrialTrove

• mohal punjab

• Medical Research Executive- backend office of citeline

  • Sep 2012 - 2015

   I have worked as Medical Research Execution Roles & Responsibilities: • Collect & analyze the information about marketed & development stage products of Bio-Pharmaceutical companies including clinical trial data, regulatory information (approvals & filings of NDA, BLA etc), press release tracking & analysis, Deal-M&A (mergers & acquisitions), patent updates capture for products & companies from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences, annual meetings (ASH, ASCO), Etc. • Competitive scientific meetings and literature coverage • Preparation of a competitive landscape for drugs, devices and clinical • Supervising, mentoring, training and management of juniors within the team • Database quality checks/assurance • Bio-pharmaceutical company coverage • Data Analysis, Data Mining & Secondary Research • Drug pipeline tracking data (Phase I, II, III & IV) • Global Meeting/conference coverage • Scientific publication analysis of molecules/receptors/technology drugs/clinical trials • MOA and Clinical/Pre-clinical data evaluation • Clinical Trial Timing Benchmarking •Accessing, analyzing and interpretation from the research clinical data. Show less