Lilly Posted September 13, 2026

Veeva Technical Lead - CTI MD Tech (GRA/GSC)

Bangalore, Karnātaka, India FULL_TIME
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Lilly is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work, but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Veeva Technical Lead - CTI MD Tech (GRA/GSC)

Global Regulatory Affairs ( GRA)  ·   Global Scientific Communications ( GSC)  ·   CTI-MD   Tech@Lilly

Veeva Vault is the platform underpinning Lilly's regulatory data, every live gateway submission depends on its object model and configuration being understood and   maintained   without disruption. The Veeva Technical Lead (R4), GRA/GSC owns the architecture and technical integrity of Veeva Vault today, while shaping the strategic vision for how regulatory systems integrations around Veeva Vault will evolve as health authority data exchange requirements advance over time. This role connects the two: safeguarding current submissions while architecting the integration patterns, schemas, and access models that position Veeva Vault's existing data as the foundation for whatever regulatory systems architecture comes next, engineered from what already exists, not invented in parallel.

Path/Level: R4 (Veeva Technical Lead)

Key Responsibilities

RIM Data Model Ownership, serve as the definitive technical authority on Veeva Vault RIM's object model, metadata, and VQL-based data access, ensuring changes preserve the integrity of live submissions.

Submission Continuity & Risk Management, support and troubleshoot the technical foundation behind active gateway submissions, ensuring configuration and data changes never jeopardize a live submission.

Future-State Architecture Vision, define and own the strategic vision for how regulatory systems integrations around Veeva Vault should evolve, positioning RIM's existing data model as the foundation that future architecture is engineered from.

Strategic Roadmap & Portfolio Alignment, connect Veeva Vault architecture decisions to the broader GRA/GSC technology strategy, ensuring investments in the platform align with enterprise AI, agentic, and digital workforce priorities.

Veeva AI & Platform Evolution Tracking, stay ahead of Veeva's own AI and automation roadmap (Vault AI and related Veeva AI capabilities), assessing how these evolving native capabilities should shape Lilly's build-vs-adopt architecture decisions.

Integration Pattern & Schema Design, architect schemas and integration contracts, including API- and MCP-based access patterns, that allow RIM data to be consumed reliably by downstream systems and emerging platforms.

Custom Integration Development, build and maintain custom integrations using the Veeva Vault SDK/APIs and Python-based automation to extend Vault capabilities and streamline manual processes.

Reusable Architecture Patterns, establish reusable architecture and design patterns around Veeva Vault that accelerate delivery, reduce duplication, and improve long-term sustainability across the RIM ecosystem.

Configuration Governance, establish and enforce configuration management, validation, and change-control discipline appropriate to a GxP-regulated Vault environment.

Data Pipeline & Systems Reliability, build and support robust data pipelines and system integrations around Veeva platforms, ensuring reliable, well-governed data flow between Vault and downstream systems.

Cross-Functional Partnership, partner with regulatory operations, data architecture, and AI/agentic engineering teams to align RIM's evolution with both near-term regulatory needs and the broader digital workforce roadmap.

Technical Mentorship, act as the go-to technical expert for the team on Vault architecture questions, raising overall data-model literacy across the organization.

Technical & Strategic Expertise Areas

Veeva Vault Architecture & Configuration · Object Models & Metadata · VQL (Vault Query Language) · Veeva Vault SDK & APIs · Systems & Data Architecture · Schema Design · API & MCP-Based Integration Contracts · Python · Java · Basic Agentic AI Concepts · Veeva AI / Vault AI Roadmap Awareness · Data Pipeline Design & Support · Cloud Platforms (AWS/Azure) · Configuration Management & Change Control · GxP/Regulated Systems Governance

Basic Qualifications

Deep expertise in Veeva Vault architecture and configuration, including object models, metadata, and VQL.

Systems/data architecture experience designing schemas and integration contracts across regulated platforms.

Proficiency in Python and Java for automation and hands-on experience with the Veeva Vault SDK/APIs for custom integrations.

Working knowledge of cloud platforms for scalable, secure architecture.

Demonstrated experience building strong, reliable systems around Veeva platforms, including designing and supporting data pipelines between Vault and downstream systems.

Basic working knowledge of agentic AI concepts (agents, orchestration, tool use) and how they apply to regulatory workflows.

Awareness of Veeva's own AI evolution (Vault AI and related Veeva AI capabilities) and its implications for future architecture decisions.

Additional Qualifications / Competencies

Familiarity with evolving regulatory data exchange requirements and how they may reshape submission systems architecture over time.

Experience partnering with AI/agentic engineering teams on platform-level technology strategy.

Track record   of evolving legacy system data models into forward-looking architectures without disrupting live operations.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

Job details

Seniority
Not listed
Function
Information Technology
Therapeutic area
Not listed
Location
Bangalore, Karnātaka, India
Employment type
FULL_TIME

How this role compares

Computed from every other active Information Technology role in our database, not just this employer's listings.

We currently track 1376 comparable Information Technology roles across 76 biopharma companies.

1376Comparable roles tracked
1216Currently active
76Companies hiring similar roles
35Countries represented

Salary context

183 of 1376 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · 2027 Business Technology Solutions Intern - Data & Software Engineering (Undergraduate) · AbbVie $21/hr – $37/hr (≈ $43,680–$76,960/yr)
Peer group range $60,320 – $400,000 (median $174,000)

Where these roles are based

Top locations among the 1376 comparable roles

India603
United States319
Spain132
Poland95
Portugal27
China21

+ 29 more countries

Seniority mix

693 of 1376 peers have a known seniority level

Senior293
Manager173
Principal59
Associate Director51
Associate48
Director38
Intern/Fellow/Postdoc14
Senior Director14
Executive/VP3

Therapeutic area mix

1 of 1376 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.