CyberOne

Techno Functional SME

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is a Techno Functional SME for a 6-month contract, offering a pay rate of "$X/hour." Remote work is available. Key skills include Model N Validata expertise, life sciences experience, and strong data analysis capabilities.
🌎 - Country
United States
πŸ’± - Currency
$ USD
-
πŸ’° - Day rate
Unknown
-
πŸ—“οΈ - Date
December 20, 2025
πŸ•’ - Duration
Unknown
-
🏝️ - Location
Unknown
-
πŸ“„ - Contract
Unknown
-
πŸ”’ - Security
Unknown
-
πŸ“ - Location detailed
San Mateo, CA
-
🧠 - Skills detailed
#Migration #"ETL (Extract #Transform #Load)" #Data Migration #SQL (Structured Query Language) #Data Governance #UAT (User Acceptance Testing) #Regression #Data Quality #Compliance #Documentation #Agile #Data Analysis #Business Analysis
Role description
The Validata Business Analyst supports Genentech’s Managed Markets and Commercial Operations by ensuring high-quality customer and membership data within the Model N Validata platform. The role focuses on roster validation, eligibility determination, customer onboarding, and compliance to minimize contract leakage, ensure accurate pricing execution, and support audit readiness. Key Responsibilities β€’ Serve as a Validata SME for Genentech’s membership validation and customer onboarding processes. β€’ Analyze and validate GPO, IDN, hospital, specialty pharmacy, and distributor rosters. β€’ Validate and maintain critical identifiers including HIN, DEA, NPI, 340B eligibility, affiliations, and address hierarchies. β€’ Support COT assignment logic and alignment with Genentech contract eligibility rules. β€’ Collaborate with Genentech business stakeholders to gather and document Managed Markets requirements. β€’ Perform data quality checks, root-cause analysis, and remediation for invalid or incomplete member records. β€’ Partner with integration and data teams to support roster ingestion, transformations, and data migrations. β€’ Execute and support UAT, regression testing, and defect resolution for Validata enhancements. β€’ Support audit requests, compliance reporting, and SOX/GxP-aligned documentation. β€’ Create and maintain SOPs, business process flows, validation rules, and training materials. β€’ Coordinate with offshore/onshore teams to ensure timely delivery and adherence to Genentech quality standards. Required Skills & Qualifications β€’ Strong experience in Life Sciences Managed Markets, preferably supporting large pharma clients. β€’ Hands-on experience with Model N Validata (mandatory). β€’ Deep understanding of: β€’ Membership & eligibility validation β€’ GPO / IDN structures and hierarchies β€’ Contract compliance, chargebacks, and pricing impacts β€’ Strong data analysis skills using Excel, SQL, or reporting tools. β€’ Experience with large-scale roster management and ongoing data maintenance. β€’ Excellent documentation, communication, and stakeholder management skills. Preferred / Nice-to-Have Skills β€’ Experience supporting Genentech, Roche, or similar Tier-1 pharma clients. β€’ Knowledge of Model N (Flex) modules. β€’ Exposure to chargebacks, rebates, and Medicaid/340B compliance. β€’ Experience working in Agile delivery models. β€’ Understanding of data governance and audit readiness frameworks.