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

- Round 1: Role-Specific Interview (India Time Zone)

- Round 2: Role-Specific Interview (US Time Zone)

- 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 recent 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.

📌 Clinical Business Analyst (Clinical BA) (Bengaluru)
🏢 PRI INDIA IT SERVICES PRIVATE
📍 Bengaluru