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Clinical Business Analyst (Clinical BA)
Ref No.: 26-00273
Location: Bangalore, Karnataka
Start Date: 13/07/2026

Experience & Availability
  • Overall Experience Required: 5–7 Years
  • Relevant Experience: Minimum 4+ Years as Business Analyst in Clinical Trials / Clinical Data Domain
  • Notice Period: Immediate Joiners or Serving Notice Period
Interview Details
  • Interview Mode: Virtual
  • Number of Rounds: 3
Interview Process
  1. Round 1: Role-Specific Interview (India Time Zone)
  2. Round 2: Role-Specific Interview (US Time Zone)
  3. Round 3: Final Managerial Round (India Time Zone)
Top Skills
  • Clinical Business Analysis (Clinical BA)
  • Clinical Trials
  • EDC / Medidata Rave
  • Functional Documentation
  • Requirements Gathering
  • Gap Analysis
  • Oracle SQL
  • Clinical Data Platforms
Must-Have Skillset
  • 5–7 years of experience as a Business Analyst.
  • Minimum 4 years of experience in Clinical Trial or Clinical Data domain.
  • Strong experience in Clinical Trials, EDC/RAVE Data, and Clinical Data Platforms.
  • Expertise in Requirements Gathering, Gap Analysis, and Functional Documentation.
  • Basic understanding and hands-on experience with Oracle SQL and table structures.
  • Strong proficiency in Excel, JIRA, and Confluence.
  • Good understanding of Software Development Life Cycle (SDLC).
  • Ability to work with stakeholders and translate business needs into functional requirements.
Good-to-Have Skillset
  • Experience with Data Transformation Rules.
  • Source-to-Target Mapping.
  • Vendor File Validation.
  • Technical and Grammatical Editing.
  • Audit Support and Compliance Documentation.
  • Understanding of Modeling Languages.
  • Ability to quickly learn new technologies and methodologies.
Key Responsibilities
  • Gather business case requirements and support pre-project activities.
  • Conduct requirements elicitation, analysis, and documentation.
  • Perform gap analysis and manage requirement traceability.
  • Facilitate UAT planning, execution, and documentation.
  • Collaborate with internal teams and external clients to resolve data-related issues.
  • Resolve conflicting business and user requirements.
  • Follow IQVIA SDLC and Computer System Validation (CSV) procedures.
  • Create and maintain User Requirement Specifications (URS).
  • Work with development teams to prepare Functional Specification (FS) documents.
  • Support process modeling and business process improvements.
  • Review Performance Qualification (PQ) documents to ensure requirement coverage.
  • Collaborate with Global IT Solutions teams for successful project implementations.
  • Work closely with developers and testers to ensure business requirements are met.
  • Develop training and support materials when required.
  • Provide regular status updates, issue tracking, and stakeholder communication.
  • Support digital transformation initiatives and continuous process improvement.
  • Ensure compliance with regulatory requirements and audit readiness activities.
Minimum Required Education
  • BE / Bachelor's Degree / Master's Degree
  • Clinical Information Management or equivalent qualification
  • B.Pharm / M.Pharm preferred
Recruiter Focus Areas
  • Hands-on experience in Clinical Trial and Clinical Data Management projects.
  • Strong exposure to EDC tools, especially Medidata Rave.
  • Experience creating BRD, FRD, URS, FS, and UAT documentation.
  • Strong stakeholder management and requirement gathering skills.
  • Knowledge of Oracle SQL and clinical data structures.
  • Experience working in regulated environments with compliance and audit requirements.
  • Excellent communication and client-facing capabilities.