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Business Analyst Resume

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New, JerseY


  • 5 years of experience in both Health care and IT industry with good work experience on Business Analysis and Drug Regulatory Affairs.
  • Business analysis experience serving as liaison between teh users and teh IT development team to determine and deliver teh most TEMPeffective solution for development and implementation including preparing detailed business requirements documents.
  • Assisted various projects from start to finish through teh SDLC process.
  • Participated in Unit Testing and UAT followed by production verification, post production testing and support.
  • Working closely with business users to define requirements, prioritize issues, and address production support issues.
  • Created UML diagrams such as use case diagrams, activity diagrams to communicate theBusiness requirements.
  • Experience in using leading industry tools like MS Visio and MS PowerPoint to develop various project deliverable.
  • TEMPEffective communicator and has teh ability to meet deadlines.


Business Analysis: Requirements Analysis, Requirement Gathering, Specifications Documentation, Product Technical Support and Training, Product Demonstration, Functional Requirement Specifications, Process Improvement, Root Cause Analysis, Research & Development, SDLC (Software Development Life Cycle), User Acceptance Testing, End User Support, Interface designs, Requirement Traceability Matrix(RTM), Manual Testing.

Tools: Microsoft Office, Windows 98 / XP, Vista, Windows7&10, Apple’s Mac. Website Watcher tool, Acrobat PDF 7.0, Basics in C - programming, MS power-point, MPP (Microsoft Project Management software), Wireframe tool.


Confidential, New Jersey

Business Analyst


  • Worked mainly in Writing requirements and documentation for web-based solutions, with strong interpersonal skills to enable interaction with clients and gathering requirements from various business areas.
  • Advanced analytical and project management skills, in-depth noledge of various phases and methodologies of software development life cycle (SDLC).
  • Presenting demo to teh clients on working software frequently during development and getting their feedback.
  • Analyzing teh impacts and feasibility of teh requirements and discussing them with teh development team and designing team. Discussing teh time and cost with teh finance team to implement teh requirements.
  • Worked on Interface (screen) Designs, by developing wireframes to visually support teh business rules and interaction requirements for a screen.
  • Monitoring teh status of bugs and bug fixes with teh development and QA teams, respectively.
  • Participating in QA team meeting and bug tracking meetings.
  • Preparing Project status report and updating to teh manager on a weekly basis and maintaining teh track of requirements in Github repository.
  • Preparing Incident reports and performing CAPA of teh reported issues.
  • Facilitating training for teh clients and end-users and resolving their queries as and when required.
  • Created Requirements Traceability Matrix to keep teh stakeholders informed of teh progress of teh project.
  • Provide technical support to teh clients and end users, if any issues are reported.

Confidential, Philadelphia PA

Associate Research Analyst


  • Worked mainly on Regulatory reportssuch as Global Regulatory Comparisons, Regulatory Intelligence Reports, Regulatory Summaries and Reference Documents.
  • Performed user trainings on editorial system functionalities/editorial processes and validatedinformation that was required to be added to IDRAC.
  • Workedjointly withregulatory consultantson six different modules namely US, EU, Canada, New Zealand, Australia and India modules.
  • Thorough noledge of regulatory filing, of IND, NDA, ANDA, BLA.
  • Good noledge on ICH and FDA regulations and In-depth noledge of teh standards, process and editorial guidelines of publication house.
  • Researched several types of documents such as clinical study reports, clinical overviews & summaries of efficacy, safety and clinical trial protocols.
  • Verified curated data according to client’s specifications.
  • Authored abstracts for teh newly published drug records along with indexing teh documents with keywords that are searchable.
  • Comprehensive noledge of scientific terminology and documentation styles.
  • Performed curation from literature covering different scientific journals and patents.
  • Experience in using website watcher tool for curation of data.
  • Performed daily surveillance of various health authority websites and official journals.
  • Maintain teh 100% interaction with teh customers by resolving teh issues in a stipulated timeframe.
  • Proactively prepared and gatheird Customer requirements and converted them into Functional Business Requirements.
  • Assign tasks to teh relevant analysts and reviewing their work.
  • Participated in client calls/meetings from time to time, to ensure meeting teh weekly targets.

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