Business Analyst – Life Sciences (Product Development) | Inductive Quotient Analytics · Teeming.ai
Inductive Quotient Analytics
Inductive Quotient Analytics (IQA) is a clinical technology company specializing in accelerating drug development through AI-driven solutions for the life sciences and healthcare industries. They…
Inductive Quotient Analytics (IQA) is a clinical technology company specializing in accelerating drug development through AI-driven solutions for the life sciences and healthcare industries. They…
Business Analyst – Life Sciences (Product Development)
On-SiteHyderabad, Telangana, IN
On-Site • Hyderabad, Telangana, IN
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Job Title: Business Analyst – Life Sciences (Product Development)Experience Required: 2-3 yearsLocation: Hyderabad-OnsiteEmployment Type: Full-timeJob Summary
We are looking for a Business Analyst to lead requirements discovery, documentation, and product alignment for our clinical platform. You will work closely with product owners, domain experts, developers, QA, and cross-functional clinical teams (Clinical Operations, Data Management, Biostatistics, and Regulatory) to understand business processes and translate stakeholder needs into clear, testable requirements and user stories that drive high-quality product delivery.
Key Responsibilities
Required Skills & Qualifications
Bachelor’s degree in Life Sciences, MBBS, Pharmacy, Biotechnology, or related field; MBA or equivalent is a plus.
At least 1 year of experience as a Business Analyst in product development within the life sciences domain.
Hands-on experience writing user stories + acceptance criteria and managing backlogs (Jira/ADO).
Engage with stakeholders, product managers, and SMEs to elicit, analyse, and document business and functional requirements.
Create and maintain BRDs/FRDs, user stories, use cases, process flows, wireframe notes (as needed), and acceptance criteria.
Perform gap analysis, impact analysis, and support requirements prioritization with stakeholders.
Partner with Engineering, QA, and UI/UX teams throughout the product development lifecycle to clarify requirements and resolve ambiguities.
Support sprint planning, backlog grooming, and feature refinement in Agile/Scrum environments.
Validate delivered features against requirements; support UAT planning, test case review, execution, defect triage, and closure.
Ensure requirements align with applicable industry standards and regulatory expectations (e.g., GxP, 21 CFR Part 11, ICH-GCP; as relevant to product).
Conduct requirements risk analysis (functional, compliance, data integrity, patient safety, security, operational) and document mitigations; escalate high-risk items early.
Perform impact and change-risk assessments for new features/enhancements, including downstream effects on workflows, integrations, validation, and releases.
Analyze customer challenges in pharma/biotech/clinical research and translate insights into product enhancements and roadmap inputs.
Develop as-is/to-be process maps and recommend process improvements aligned with product and user goals.
Support analysis of KPIs/metrics, reporting requirements, and usability improvements to drive adoption and efficiency.
Prepare product demos, functional walkthroughs, release notes inputs, and training/UAT support materials.
Maintain documentation hygiene: timely updates, version control, traceability, and proactive stakeholder communication.
Strong understanding of pharma R&D, clinical workflows, regulatory processes, or related functional areas.
Experience in documenting compliance-related requirements (21 CFR Part 11,HIPAA, GxP, etc.).
Proficiency in tools such as Azure DevOps, Visio, or similar.
Ability to create detailed functional specifications and user stories.
Strong analytical, documentation, and problem-solving skills.
Excellent communication and stakeholder management abilities.
