Headline

Senior Business Analyst | Healthcare SaaS | Pharmacovigilance | MedDRA & WHO-DD | Remote

About

I’m a Senior Business Analyst with 5+ years of experience working at the intersection of Healthcare, Pharmacovigilance, and regulated SaaS platforms. I specialize in translating complex clinical and regulatory workflows into scalable product requirements that drive compliant and high-quality software delivery. My core strength lies in owning the full requirement lifecycle — from stakeholder discussions and BRD/FRD creation to user stories, acceptance criteria, system validation, and end-to-end UAT across global pharmacovigilance products. At RxLogix, I have led functional validation and product quality initiatives for PV SaaS platforms used by pharmaceutical clients worldwide. I work closely with Product Managers, Engineering, and QA to ensure regulatory-aligned releases while improving system accuracy, data integrity, and coding efficiency. I bring hands-on expertise in: • Pharmacovigilance workflows (CIOMS, MedWatch, case lifecycle) • MedDRA & WHO Drug Dictionary intelligent coding validation • GxP & 21 CFR Part 11 compliant systems • Requirement documentation (BRD, FRD, RTM, user stories) • SQL-based data validation & API/JSON verification • Agile product collaboration across distributed teams Beyond functional analysis, I actively contribute to product improvements by identifying workflow gaps, validating integrations, and mentoring analysts on quality-driven delivery. I’m currently exploring remote Senior Business Analyst / Product & Systems Analyst roles within Healthcare, Life Sciences, and SaaS organizations where regulatory understanding and strong product thinking are critical to building reliable, high-impact platforms. Let’s connect if you’re building products in Healthcare, Pharma, or regulated SaaS and need someone who understands both domain complexity and product execution.

Location

Noida

Work experience

Quality Business Analyst at RxLogix Corporation, Apr 2025 - Present · 1 yr 2 mos, Noida, Uttar Pradesh, India, Partner with product, QA, and engineering teams to refine business requirements and improve Pharmacovigilance (PV) system performance. Lead UAT, functional testing, and regulatory validation across HealthTech modules. Conduct SQL-based defect and impact analysis, prioritizing fixes and streamlining releases. Enhance MedDRA and WHO-DD integration workflows, reducing data errors by 15%. Mentor junior analysts in requirement validation, JIRA management, and root cause analysis. Use Confluence for documentation and design reviews, improving release speed by 10%.

Associate Clinical Data Analyst II at Rx Logix Corporation Pvt. Ltd., Sep 2022 - Mar 2025 · 2 yrs 7 mos, Noida, Uttar Pradesh, India, 1. Ticket Analysis & Form Configuration: Analyze Jira tickets and understand form configurations and coding requirements based on client specifications. 2. Form Configuration Development: Executing form configuration tasks and developing Python code to ensure accurate data extraction. 3. API Testing & Deployment: Use Postman for thorough API testing, ensuring data accuracy through JSON and Python file deployments in Docker environments. 4. Build Management: Oversee the creation of builds and manage documentation for deployment approval. Responsible for uploading builds and linking them to relevant Jira tickets. 5. Issue Resolution: Address issues in data extraction and software functionality, implementing testing procedures and improving data accuracy and software performance. 6. Scrum Participation: Attend scrum meetings, provide progress updates, and collaborate with cross-functional teams for efficient issue resolution and deployment support.

Associate Clinical Data Analyst at Rx Logix Corporation Pvt. Ltd., Sep 2021 - Sep 2022 · 1 yr 1 mo, Noida, Uttar Pradesh, India, 1. API Testing with Postman: Conduct thorough API testing, validating clinical data by checking accuracy and parsing compliance with documentation requirements. 2. Data Discrepancy Resolution: Collaborate with developers to resolve discrepancies in clinical trial data, providing feedback for prompt issue resolution. 3. Adverse Event Form Validation: Validate adverse event forms through Postman, ensuring their accuracy before data integration into clinical systems. 4. Iterative Testing: Implement and execute iterative rounds of testing to ensure continuous improvement in data accuracy and system functionality.

Data Tagger at Rx Logix Corporation Pvt. Ltd., Sep 2020 - Sep 2021 · 1 yr 1 mo, Noida, Uttar Pradesh, India, 1. Clinical Data Tagging: Categorized and tagged clinical data, including patient information, medical histories, and adverse event data. 2. Regulatory Compliance: Ensured clinical data tagging and categorization adhered to FDA, EMA, and ICH-GCP guidelines. 3. Optimization of Data Tagging: Enhanced clinical data management using tools like Prodigy and Putty, improving the tagging process and increasing productivity. 4. Data Integrity: Maintained the integrity of tagged clinical data to ensure it met regulatory standards for clinical trial reporting. 5. Collaboration with Developers: Worked closely with developers to enhance data tagging processes, streamline workflows, and improve overall data accuracy.

Education

Bsc nursing, Medical student, Fh medical college