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Business Analyst/PM - Clinical Data

Tanisha Systems

Morrisville, CA

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JOB DETAILS
SALARY
$120,000–$130,000 Per Year
JOB TYPE
Full-time, Employee
SKILLS
Acceptance Testing, Agile Programming Methodologies, Artificial Intelligence (AI), Atlassian JIRA, Benchmarking, Biology, Biostatistics, Biotech and Pharmaceutical, Business Analysis, Business Intelligence, Clinical Data, Clinical Data Interchange Standards Consortium (CDISC), Clinical Data Management, Clinical Trial, Cloud Computing, Code of Federal Regulations, Computer Science, Cross-Functional, Data Analysis, Data Processing, Data Quality, Data Sets, DevOps, Documentation, Environmental Sciences, Error Handling, FDA (Food and Drug Administration), GitHub, GxP, HIPAA (Health Insurance Portability and Accountability Act), Healthcare, Identify Issues, Information/Data Security (InfoSec), Maintain Compliance, Microsoft Certifications, Microsoft Product Family, Microsoft Windows Azure, Power BI, Predictive Modeling, Problem Solving Skills, Progress Reports, Python Programming/Scripting Language, Quality Assurance, Quality Monitoring, R Programming Language, Regulations, Regulatory Compliance, Regulatory Submissions, Reporting Dashboards, Requirements Management, Requirements Validation/Verification, Scorecarding, Scrum Project Management and Software Development, Standard Operating Procedures (SOP), Statements on Auditing Standards (SAS), Statistical Analysis System (SAS), Validation Documentation
LOCATION
Morrisville, CA
POSTED
11 days ago
Business Analyst/PM - Clinical Data
Morrisville, NC 27560 - Onsite Role - Prefer local candidates
Salary – Market (DOE)
FTE role

We are looking for a seasoned Business Analyst with experience in requirement analysis and delivery of data & analytics solutions for regulated industries (Life Sciences / Pharma). The ideal candidate will drive requirement gathering, compliance alignment, and stakeholder engagement for a GxP-compliant, cloud-native data platform on Microsoft Fabric and Azure. Success will be measured by the ability to translate CDM/Biostatistics needs into validated pipelines, dashboards, and audit-ready documentation. The Business Analyst acts as the bridge between clinical stakeholders and technical teams, ensuring requirements are captured, translated, and delivered effectively. Leads requirement gathering & documentation across CDM, Biostatistics, and vendor partners. Translates business and regulatory needs into functional specifications aligned with 21 CFR Part 11, GxP, and HIPAA. Supports validation frameworks, audit-ready documentation, and reporting requirements such as Power BI dashboards and compliance scorecards. Facilitates workshops, UAT sessions, and milestone signoffs to secure stakeholder alignment. Prepares for future readiness, advanced analytics, and AI-driven insights.

Skills / Experience
  • 10+ years in IT with 6+ years in Business Analysis for regulated environments (Life Sciences, Pharma, Healthcare, Clinical Data Management, Biostatistics).
  • Proven ability to gather, document, and validate requirements; conduct workshops; create functional specifications; ensure compliance with FDA 21 CFR Part 11, GxP, HIPAA
  • Knowledge of regulatory frameworks including 21 CFR Part 11, GxP, HIPAA, GDPR; experienced in IQ/OQ/PQ documentation, SOPs, and audit-ready deliverables
  • Strong domain knowledge in CDM, Biostatistics workflows, CDISC (SDTM/ADaM), FDA eCTD; Tools: GitHub Projects, DevOps board, Jira, Power BI, Microsoft Fabric
  • Understanding of Microsoft Fabric, governance policies, compliance documentation; exposure to BI solutions using Power BI
  • Exposure to CDISC/SDTM/ADaM standards, OMOP mapping, advanced analytics (R, Python, SAS), and AI-driven accelerators (WinAIDM)
  • Skilled in stakeholder engagement, workshops, UAT sessions, and cross-functional collaboration
  • Experience defining validation rules, monitoring dashboards, and exception handling processes
  • Experience leveraging GenAI tools (GitHub Copilot, Microsoft Fabric Copilot, M365 Copilot)
  • Bachelor’s degree in Life Sciences, Computer Science, or related field
Role / Job Description
  • Requirements Analysis & Translation – Lead requirement gathering sessions; translate regulatory and business needs into functional specifications; document user stories, acceptance criteria, and workflows; author BRD and FRS
  • Data Governance & Compliance – Define validation rules; ensure dataset versioning, lineage, audit trails, and electronic signatures; collaborate with QA teams for validation documentation and SOPs; support compliance reviews and inspection readiness
  • Analytics & Reporting Enablement – Capture reporting requirements for Power BI dashboards, compliance scorecards, and study progress reports; define business rules for secure analytics environments; ensure reporting aligns with governance and audit workflows
  • Stakeholder Engagement & Delivery – Facilitate workshops, UAT sessions, and requirement walkthroughs; act as liaison between business stakeholders and technical teams; drive milestone sign-offs for requirement validation and compliance readiness
  • Operational Oversight & Vendor Collaboration – Define secure vendor data exchange requirements; monitor data quality dashboards; coordinate issue resolution; ensure scalability and performance benchmarks
  • Future Readiness – Contribute to roadmap planning for CDISC/SDTM/ADaM integration, OMOP mapping, advanced analytics, and AI-driven insights
  • Communication & Troubleshooting – Build productive relationships across teams; provide feedback during workshops; troubleshoot requirement gaps, compliance risks, and process inefficiencies; work in Agile/Scrum projects with Jira or Azure DevOps
  • Secondary Skills / Good to Have – Life Sciences domain knowledge, deeper knowledge of clinical data flows, CDISC standards, regulatory submission processes, vendor data exchange practices
  • Advanced Analytics & AI Exposure – Awareness of AI-driven accelerators (WinAIDM, Fabric Copilot); exposure to RWE and predictive modeling in clinical trials
  • Certifications / Good to Have – CBAP, PMI-PBA, IIBA; Microsoft certifications (DP-600, DP-203)
Expected Outcomes
  • Phase 1 Clinical Data Repository delivered within 16–18 weeks; requirements translated into compliant workflows and validated pipelines; audit-ready documentation completed.
  • Power BI dashboards and compliance scorecards actively used by stakeholders; improved collaboration across CDM, Biostatistics, IT, and vendors; foundation established for Phase 2 (CDISC/OMOP integration, advanced analytics, AI-driven insights).

This Role Matters
  • Ensures regulatory confidence by embedding compliance into every requirement; Drives operational efficiency by reducing manual data transfers and enabling secure vendor collaboration
  • Enables analytics readiness by defining requirements for dashboards, scorecards, and validated pipelines; Fosters stakeholder alignment through workshops, UAT sessions, and milestone signoffs
  • Lays the foundation for innovation, preparing the organization for CDISC/OMOP integration, advanced analytics, and AI-driven insights

About the Company

T

Tanisha Systems

INDUSTRY
Computer Software