11-Jul-2026
Delhi (DL), 1
Full Time
Huntsman
???? Location: India
???? Job Type: Permanent
Manage PV Configuration Standards, including:
Distribution Rules
Study Configurations in LSMV, LSR, and EV Triage modules
Handle PV system configurations for:
Company Products
Clinical & Post-Marketed Studies
Business User Roles & Data Privacy
Code Lists, Libraries, MedDRA, WHO
Distribution Rules, Accounts & HA Destinations
E2B Profiles, SDEA Profiles & Gateways
Maintain E2B Gateways with Health Authorities and Business Partners
Support Data Migration and Ingestion Requests
Perform User Acceptance Testing (UAT) for configuration changes
Document configuration changes in collaboration with business users
Facilitate training sessions and update training materials
Provide Safety Data and Ad-hoc Reports during audits and inspections
Collaborate with digital vendor teams for configuration changes, testing, and deployments
Work in an Agile environment
6–8 years in the pharmaceutical industry, particularly with GxP systems
Proven background in:
Pharmacovigilance system operations
PV Databases (e.g., Argus, Aris-G, VAULT Safety, LSMV)
Configuration management and documentation
IS and validation processes
Safety reporting compliance (CIOMS, EudraVigilance, FDA REMS)
Proficient in:
SQL / PL-SQL
Microsoft Office (Excel, Word, PowerPoint)
Business Intelligence Tools: Power BI, Spotfire
Familiar with ICH GVP, GxP, and regulatory safety requirements
Experience with UAT, system upgrades, and data migration
Cross-functional communication with Clinical, Regulatory, and Medical Affairs teams
Process Improvement experience is a plus
Strong stakeholder management, negotiation, and global collaboration skills
High attention to detail, analytical thinking, and problem-solving abilities
Excellent organizational and project management capabilities
Effective communicator across multicultural environments
Team player with strategic leadership potential
Bachelor's in Pharmacy / Life Sciences / Engineering (or equivalent)
Fluency in English (verbal and written)
This role is a strategic opportunity for experienced professionals in pharmacovigilance systems who want to contribute to global drug safety compliance through expert configuration and data management practices.
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