Full-Time

Engagement Manager

R&D Business Consulting

Updated on 5/31/2026

Veeva Systems

Veeva Systems

5,001-10,000 employees

Cloud-based quality, regulatory, and claims management

No salary listed

Paris, France

Hybrid

Hybrid work; work from home or office on any given day.

Category
Business & Strategy (1)
Required Skills
Veeva
Requirements
  • Experience 8+ years in Life Sciences Consulting (Business or Management Consulting preferred)
  • Leadership: Proven track record of managing large project teams and $1M+ engagements
  • Domain Knowledge: Proven expertise in Clinical Data/Operations, Regulatory or Pharmacovigilance/Drug Safety and the broader Life Sciences industry
  • Mindset: A highly analytical approach to problem-solving with the ability to influence C-suite stakeholders
  • Education: Bachelor’s degree or higher
Responsibilities
  • Strategic Delivery: Act as the end-to-end lead on Veeva’s most complex, large-scale, and global engagements
  • Account Leadership: Build and navigate senior customer relationships, leading proposals for significant project wins and driving long-term account strategy
  • People Leadership: Lead and inspire teams of 4+ consultants across multiple projects simultaneously, fostering a culture of excellence
  • Financial Oversight: Manage project budgets of $1M+, acting as the primary point of contact for project health and commercial success
  • Practice Building: Support brand-building activities and the development of internal IP to keep Veeva Business Consulting at the forefront of the industry
Desired Qualifications
  • Deep knowledge of Veeva products
  • Experience delivering SaaS or Tech-enabled consulting solutions

Veeva Systems provides cloud-based software that helps consumer goods and chemical companies manage quality, regulatory compliance, and advertising claims. The platform works by connecting different departments—from the supply chain to marketing—to provide a single source of data that tracks a product's journey and ensures it meets safety standards. Unlike competitors that offer general business tools, Veeva specializes in navigating the highly complex regulations originally found in the life sciences sector and applies that specific expertise to other regulated industries. The company's goal is to help businesses bring safe, sustainable, and compliant products to market faster by providing end-to-end visibility and traceability.

Company Size

5,001-10,000

Company Stage

IPO

Headquarters

Pleasanton, California

Founded

2007

Simplify Jobs

Simplify's Take

What believers are saying

  • Falcon can automate trial intake, health-authority correspondence, and safety triage.
  • Snowflake integration expands analytics and AI around validated Vault data.
  • Ostro and Vault AI Tab deepen compliant conversational engagement and governed search.

What critics are saying

  • Salesforce Agentforce Life Sciences already targets 140+ life-sciences customers.
  • Falcon arrives in November 2026, leaving Salesforce a selling-cycle advantage.
  • External AI copilots can relegate Veeva to back-end record keeping.

What makes Veeva Systems unique

  • Veeva controls a unified Vault stack across commercial and development workflows.
  • Its standard agents run in-context inside regulated applications, preserving deterministic compliance.
  • Vault CRM, Safety, Quality, and Falcon target specific life-sciences workflows.

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Your Connections

People at Veeva Systems who can refer or advise you

Benefits

Parental leave

PTO

Free food

Health, dental, & vision insurance

Gym membership reimbursement

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Drug Discovery & Development
Jun 1st, 2026
Salesforce lands 140 life sciences clients, pitches 'headless' AI to pharma.

Salesforce lands 140 life sciences clients, pitches 'headless' AI to pharma. A patient support program engagement run as a remote call, with meeting controls for audio, screen share and recording alongside the approved deck. (Image: Salesforce) As Peter Gassner, CEO of Veeva Systems, the influential cloud software provider for the life sciences industry, took the stage at the Veeva Commercial Summit in Boston, Salesforce announced that more than 140 life sciences organizations are using its competing Agentforce Life Sciences platform. In the mix as Salesforce clients are several marquee industry names like Novartis, AstraZeneca, Moderna and Merck Animal Health. "The 140 represents customers across our entire portfolio," said Joe Ferraro, SVP and GM of life sciences at Salesforce, "regardless of whether they are using it for patient engagement, clinical engagement, commercial engagement or medical engagement." Salesforce is positioning Agentforce Life Sciences as a broad, AI-native platform across clinical, medical, patient and commercial engagement. So is Veeva. As Gassner put it at the Commercial Summit: "The Agentic Commercial model changes everything about how we approach commercialization." For example, he pointed to everything "from digital and non-personal promotion," how field teams operate as well as content approval and creation. 'Everybody is using agents' When asked about how Salesforce's agentic AI strategy compares to Veeva's, Ferraro said, "Everybody is using agents now. Salesforce has been pioneering AI for the last decade, whereas many legacy systems have been slow to innovate. I would say a combination of our product vision two years ago, when we started this process of [building Agentforce Life Sciences], and customer pressure really forced Veeva's hand on this." Ultimately, Ferraro differentiates Agentforce Life Sciences from Veeva's offerings in terms of experience. "We are talking apples and oranges," he said. "We have been in the AI game at Salesforce since the predictive and machine-learning days." Salesforce CEO Marc Benioff may have ramped up Salesforce's AI focus in the wake of the ChatGPT launch, but the history goes back further. At an internal all-hands in 2014, he declared Salesforce an "AI-first company", the same year it acquired the machine-learning startup RelateIQ for $390 million, and Salesforce launched Einstein, its first CRM AI, at Dreamforce in 2016. In the years since, Benioff has made autonomous agents the company's central pitch, launching the Agentforce platform at Dreamforce in September 2024, branding it "digital labor," and setting a goal to empower one billion agents by the end of 2025. That focus has not died down. On the company's first-quarter fiscal 2027 earnings call on May 27, Benioff told investors Salesforce had processed 28.6 trillion AI tokens, up 152% quarter over quarter, and called agentic AI "the biggest growth opportunity" for the company since it brought CRM to the cloud, with Agentforce annual recurring revenue at $1.2 billion. "We have thousands of engineers working on AI at Salesforce right now," Ferraro said. "There is nowhere near that scale for Veeva, so we are able to move a lot faster from an agentic standpoint." For its own part, Veeva announced Falcon on May 27, an agentic platform and set of standard agents for drug development that run in Veeva Development Cloud across its clinical, regulatory and safety applications, with early-adopter availability set for November 2026. Gassner called it the company's "first offering in agentic labor." Vault CRM's Free Text, Voice, and Pre-call agents went live in December 2025. Veeva's public roadmap listed Safety and Quality agents for April 2026, and its 26R1 release introduced a Narrative Agent for Veeva Safety. Veeva has been buying as well as building. In March 2026 it acquired Ostro, an AI brand-engagement platform for life sciences, for about $100 million. The acquisition adds conversational AI that answers patient and HCP questions from Medical, Legal, and Regulatory (MLR)-approved content rather than generating novel responses. At its Commercial Summit event, Gassner previewed a Vault AI Tab coming in August, coming in August, a conversational layer that answers questions against a customer's Vault data within existing security permissions. The Agentforce Life Sciences home screen, where a user queries the assistant with prompts such as "HCPs to meet with next" or "Show me declining prescribers." (Image: Salesforce) The bet on 'headless' The larger agentic strategy is what Salesforce calls "headless." Ferraro described it as "popping the top off the platform, exposing all the APIs, and exposing all the data models and workflows as MCP tools," referring to the Model Context Protocol standard that Anthropic introduced in 2024. MCP has since been donated to the Agentic AI Foundation, a Linux Foundation directed fund, in December 2025. Rather than requiring users to work inside Salesforce's own interfaces, the company exposes its productized workflows as MCP servers that surface inside whatever AI tool a customer already uses. "I was with a customer yesterday who has made a significant investment in Anthropic, and they are going to use our MCP service for Agentforce Life Sciences to bring all of those compliant workflows directly inside Claude," Ferraro said. Meanwhile, Veeva's Vault AI Agents are built to run inside Veeva's own applications, working in-context against its data, documents, and workflows, a depth-inside-the-app posture rather than a surface-it-anywhere one. Publicly visible examples of connectors that expose Veeva data to outside models today include third-party offerings such as CData. The two also split on the model layer. Salesforce supports a range of Salesforce-managed and customer-supplied models for Agentforce. Veeva fixes the model layer for its standard agents, Vault CRM's included, running them on Anthropic and Amazon models hosted on Amazon Bedrock, and opens model choice only for custom agents, where customers can use Veeva-hosted models or bring their own on Bedrock or Microsoft Azure AI Foundry. Agents help speed onboarding. Salesforce has noted that some of its smaller life science customers have completed onboarding in about a month. Meanwhile, companies like Chiesi and CSL are using Salesforce to unify customer data and coordinate engagement across commercial and medical operations. In terms of the rapid onboarding, agents deserve part of the credit, Ferraro said, reducing the need for large teams of consultants to oversee the process. "You get one forward-deployed engineer, and they can do the work of five or 10 previously, because they have Claude Code, or they have Codex, and they can point those tools at the Salesforce platform," he said. For instance, Salesforce built an MCP server inside Agentforce Life Sciences that configures the product itself. A request like adding a quick action to the iPad app that launches a prompt in the UI, a task a human would handle by navigating through nested configuration screens, gets executed by the agent automatically. A rep's in-visit view in Salesforce's life sciences customer-engagement app with sample content. (Image: Salesforce) Large models are probabilistic by design, trained to predict likely next tokens from context. That can help summarize a long PDF in seconds, but life sciences workflows demand predictability: how often a rep can message a physician, what the message says, and whether consent exists are all regulated. For that reason determinism is the core theme hanging over agentic software in regulated industries. On compliance, Salesforce and Veeva land in a similar place. Salesforce uses a feature it calls Agent Script to weave deterministic checks, approved templates and consent status into the probabilistic layer. Meanwhile, Veeva runs its standard agents in-context inside its own applications against its data and workflows. As a result, the model can synthesize and surface, but the regulated action runs through a fixed set of tools backed by deterministic workflows and confined actions. "[The model] cannot go off script, because those tools are unavailable," Ferraro said. "The tools are outside its toolbox."

Compliance in Pharma
Apr 10th, 2026
Validfor vs Veeva Vault QMS: which QMS platform is better in 2026?

Validfor vs Veeva Vault QMS: which QMS platform is better in 2026? Last updated: April 10, 2026 9:46 am Quality Management Systems (QMS) are essential for organizations in regulated industries such as pharmaceuticals, biotechnology, and medical devices. Choosing the right platform affects compliance, operational efficiency, and long-term scalability. In this comparison, Compliance in Pharma explore Validfor and Veeva Vault QMS to help you determine which solution best fits your needs. Overview of Validfor. Validfor is a modern validation-focused platform built with an automation-first approach. It focuses on continuous compliance, workflow automation, and reducing manual validation effort. Validfor is ideal for organizations seeking speed, flexibility, and efficiency. Overview of Veeva Vault QMS. Veeva Vault QMS is a cloud-based QMS platform designed specifically for life sciences. It provides comprehensive quality management capabilities, including document control, training, CAPA, and audit management. Veeva Vault QMS is widely used by global pharmaceutical and biotech companies. Key differences. 1. Platform focus. Validfor is primarily focused on validation automation and continuous compliance. Veeva Vault QMS is a full QMS platform covering all quality processes. 2. Automation. Validfor is built with automation at its core, enabling real-time validation and reduced manual effort. Veeva Vault QMS offers automation across quality processes but follows a more structured QMS framework. 3. Ease of use. Validfor provides a modern, user-friendly interface designed for fast adoption. Veeva Vault QMS has a robust interface but may require training due to its extensive features. 4. Implementation speed. Validfor is designed for rapid deployment and quick onboarding. Veeva Vault QMS implementations can take longer, especially in large enterprises. 5. Scalability. Both platforms are highly scalable. Validfor is well-suited for agile teams, while Veeva Vault QMS is optimized for large global organizations. 6. Compliance. Both platforms support GxP and regulatory compliance. Veeva Vault QMS has a strong track record in life sciences, while Validfor emphasizes continuous compliance through automation. Pros and cons. Validfor. * Automation-first approach * Fast implementation * Modern and intuitive interface * Continuous compliance capabilities * Limited full QMS functionality Veeva Vault QMS. * Comprehensive QMS features * Strong life sciences specialization * Global scalability * Longer implementation time * More complex setup and usage Which one should you choose? The best choice depends on your organization's scope and priorities. * Choose Validfor if: You want automation, speed, and validation-focused workflows * Choose Veeva Vault QMS if: You need a full QMS platform for enterprise-scale operations Final thoughts. Validfor and Veeva Vault QMS serve different roles within regulated environments. Veeva Vault QMS provides a comprehensive, enterprise-grade QMS solution, while Validfor represents a modern, automation-driven approach to validation. By aligning your choice with your operational needs, you can achieve better compliance, efficiency, and scalability. In recent years, validation processes across the pharmaceutical industry have been undergoing a major transformation. Workflows that were traditionally managed through paper documentation, spreadsheets and manual review cycles are increasingly moving toward digital validation platforms. As a result, life sciences organizations often evaluate solutions such as Kneat, Validfor, ValGenesis, MasterControl and Veeva when modernizing validation lifecycle management and compliance documentation. News & research. Audit management is a vital process in regulated industries such as pharmaceuticals, biotechnology, and medical devices. Organizations must plan, execute,... April 10, 2026 Validfor is rapidly emerging as a next-generation digital validation platform, designed to address the evolving needs of modern pharmaceutical and... April 10, 2026 Inspection readiness is about retrieval speed During an inspection, the biggest risk is not the absence of controls. It is... April 9, 2026 In highly regulated industries, validation and quality management systems play a critical role in ensuring compliance, product quality, and operational... April 9, 2026

Missouri Southern State University
Apr 8th, 2026
Missouri Southern to host Global Leaders Speaker Series, featuring Dr. Monicca Shanthanelson.

Missouri Southern to host Global Leaders Speaker Series, featuring Dr. Monicca Shanthanelson. Missouri Southern State University (MSSU) will host the Global Leaders Speaker Series on Monday, April 13, in the Ron Richard Athletic Center from 6 p.m. to 8 p.m. The event is free and open to the public. The series aims to inspire and inform attendees interested in scientific innovation and global leadership to build a more connected world. 0This event will feature a keynote address by Dr. Monicca Shanthanelson, a global Medical Affairs executive with more than 15 years of experience in enterprise medical strategy, scientific communications, and organizational leadership across oncology and neuroscience. She holds a PhD in Neuroscience from Stony Brook University and earned dual undergraduate degrees in Biology and Chemistry from Missouri Southern State University. "Giving our students the opportunity to hear from experts in a diverse set of fields lets them learn leadership and global citizenship skills from people who have lived experience in both of those areas," said Benjamin Cooper, MSSU's Director of Global Leaders. "Bringing Dr. Shanthanelson back to the MSSU campus is an exciting opportunity for them to learn from someone who was once in their position and has gone on to have global reach in her career." She currently serves as Scientific Director of Cross-Oncology Strategy within Global Medical Affairs at AbbVie, where she leads initiatives that align medical teams across international markets. In her many impressive roles, Dr. Shanthanelson has developed global frameworks to expand the reach of clinical data and improve coordination across major groups. Her work has contributed to measurable operational efficiencies and the adoption of standardized practices across global oncology teams, making a true impact. Prior to joining AbbVie, Dr. Shanthanelson served as Vice President and Global Head of Medical Affairs Business Consulting at Veeva Systems. There, she advised life sciences organizations and executive Medical Affairs leaders on global strategy, omnichannel engagement transformation, insight generation, and digital enablement of scientific exchange while owning profitability and client satisfaction. She also held senior leadership roles at MedThink SciCom (now FingerPaint Medical) where she supported pharmaceutical clients worldwide. With her impressive array of accomplishments, attendees of the Global Leaders Speaker Series are guaranteed to walk away with fresh insight from Dr. Shanthanelson. About Global Leaders Speaker Series Missouri Southern's Global Leaders Speaker Series reflects the university's ongoing commitment to fostering global perspectives and connecting students and the community with leaders and visionaries shaping the future of their industries. Through events like this, the university continues to create spaces and opportunities for meaningful dialogue, propagating students' learning and engagement beyond the classroom. For more information about the Global Leaders program, visit the program webpage.

Yahoo Finance
Mar 14th, 2026
Veeva Systems posts 13.6% CAGR since 2013 IPO amid growing cloud competition

Veeva Systems, a cloud solutions provider for the life sciences industry, has delivered a 13.6% compound annual growth rate since its 2013 IPO. The company serves 15 of the top 20 biopharma companies and benefits from high switching costs, as clients depend on its platform for critical functions like clinical trial data management and regulatory compliance. Despite revenue growth slowing as the company matures, Veeva estimates its total addressable market at $20 billion against trailing-12-month revenue of $3.2 billion. The company is also expanding into new sectors including cosmetics, consumer packaged goods and chemicals. To turn a $70,000 investment into $2 million over 30 years would require an 11.82% CAGR, slightly below Veeva's historical performance but achievable given its market position and growth opportunities.

Yahoo Finance
Mar 13th, 2026
Veeva Systems fair value estimate cut to $270.93 as analysts trim targets amid software sector pressure

Veeva Systems' fair value estimate has been cut from $302.60 to $270.93, a roughly 10% reduction reflecting more cautious assumptions. The adjustment comes amid mixed analyst sentiment, with firms trimming price targets despite pointing to strong Q4 execution and solid profitability. Several analysts, including Citi, TD Cowen and Piper Sandler, highlighted Veeva's strong Q4 performance, with billings and guidance exceeding consensus and operating margins reaching 43.8%. Some firms view Veeva as well-positioned against AI-related risks due to its integrated platform. However, Goldman Sachs maintains a Sell rating with a $190 target, citing concerns around CRM competition and AI positioning. Multiple firms have lowered targets due to software sector compression and scepticism around growth sustainability. Morgan Stanley upgraded to Equal Weight in February.