Jobs at Pfizer

Lead hands-on configuration and solution design for Veeva Vault RIM across assigned domains. Own release impact assessments, manage end-to-end delivery in a SAFe Agile team, ensure CSV/GxP compliance and audit readiness, enable integrations and data flows, provide technical guidance and mentoring, and drive configuration standards, governance, and quality for global regulated deployments.

The Associate Manager - Indirect Taxation at Pfizer will manage GST compliance, audits, reconciliations, and indirect tax matters, serving as the key operational owner and ensuring adherence to regulations.

Field-based pharmaceutical sales role responsible for achieving territory sales budgets through HCP engagement, sales planning, analytics, retailer and hospital coordination, KOL management, compliance with SOPs (including adverse event reporting), executing promotional campaigns, mentoring trainees, and using technology for field operations and reporting.

Perform clinical data monitoring and management activities: data review, query management, investigate logic checks, and ensure database design quality through documentation, testing, validation, and implementation of data collection tools. Act as first point of contact for CTMS issues, follow SOPs, collaborate to resolve TMF/document discrepancies, and contribute to process improvements and project work.

Lead and coordinate CDIS deliverables for clinical trials, ensuring data quality, standards adherence, TMF documentation, inspection readiness, and oversight of Data Managers while partnering with cross-functional teams and external vendors to meet study timelines.

The Manager - Direct Tax will oversee Direct Tax compliance, assessments, litigation, and support transfer pricing in India, coordinating with external consultants and managing tax obligations within a pharmaceutical context.

Field-based pharmaceutical commercial role responsible for achieving territory sales budgets through planning, sales calls to doctors/chemists/hospitals, KOL engagement, competitor intelligence, order booking, promotional campaigns, CME events, adverse-event reporting, team mentoring, and adherence to Pfizer policies and reporting processes.

Lead strategy, architecture, implementation, and operations for enterprise authentication (SSO, MFA, passwordless, federation) across on-prem, cloud, and hybrid environments. Collaborate with security, cloud, dev, and business teams; manage vendor selection, incident response, compliance (GDPR, HIPAA, NIST, SOX, GxP), KPIs, and user experience improvements while leading and scaling IAM engineering and operations.

Develop and deliver analysis-ready datasets, tables, listings, and figures for clinical studies using statistical programming. Ensure high-quality code, documentation, and QC; collaborate with statisticians and leads; apply ICH and regulatory standards and clinical data standards to support study and asset-level deliverables.

Support clinical data monitoring and management activities including data review, query management, validation, and resolving data/document discrepancies. Provide first-line CTMS support, ensure database and documentation quality, follow SOPs, and contribute to process improvements and projects.

Lead design and delivery of end-to-end data architectures and reusable data products for global logistics. Translate business needs into scalable data models, integrations (TMS/WMS/ERP/IoT), and pipelines. Ensure data quality, lineage, compliance (GxP, SOX), migrations, platform consolidation, and enable analytics/AI consumption. Mentor teams, govern architecture standards, and minimize disruption during system transformations.

Lead design, configuration, and lifecycle management of Veeva Vault RIM across domains. Translate requirements into secure, compliant Vault configurations, support integrations, enable testing/validation (CSV/GxP), and deliver releases on a SAFe Agile team while providing technical guidance and stakeholder partnership.

Lead scientific and strategic AI efforts for Vaccines Medical: define AI vision and roadmap, govern responsible AI standards, prioritize and deliver validated AI-enabled solutions, partner cross-functionally, oversee deployment and adoption, manage budget and vendors, and ensure regulatory, ethical, and scientific compliance across global medical affairs.

Develops, reviews, and quality-checks global medical affairs content (manuscripts, abstracts, posters, slide decks, multimedia) for assigned therapeutic area. Manages projects end-to-end, trains and mentors junior staff, liaises with stakeholders (graphics, compliance, statistics), ensures timelines, quality, and compliance, and adopts new tools including generative AI to improve content creation.