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Veeva Salaries Jobs (NOW HIRING)

Director - Veeva Regulatory

Boston, MA · On-site

$125 - $300/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The salary range listed here has been provided to comply with local regulations and represents a ... Veeva is an equal opportunity employer. All qualified applicants will receive consideration for ...

Veeva Clinical Consultant

Nashville, TN · Hybrid

$70K - $196K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

You are: An experienced Veeva Clinical Consultant The work: Designing, configuring, and ... Employee Benefits | Accenture ( Role Location Annual Salary RangeCalifornia $70,350 to $196 ...

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Veeva Salaries information

Does Veeva pay well?

Veeva salaries for roles such as software developers, consultants, and project managers are generally competitive within the industry, often aligning with market standards for technology and life sciences companies. Compensation can vary based on experience, location, and specific job responsibilities, and benefits typically include health insurance, bonuses, and stock options. Overall, Veeva is considered to offer fair and competitive pay for its employees in relevant roles.

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Infographic showing various Veeva Salaries job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Director - Veeva Regulatory

Veeva Systems, Inc.

Boston, MA • On-site

$125 - $300/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Veeva Systems rating

7.6

Company rating: 7.6 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

154th of 244 rated software companies


Job description

The Role

You are the definitive authority on Regulatory Information Management (RIM) for Veeva. This is not a people‑management role; it is a Mastery-level position. You will bridge the gap between complex regulatory requirements and modern software solutions. In this role you will be responsible for growing Veeva’s Regulatory product market share.

Why This Role is Unique
  • Influence, Not Admin: You aren't managing a team's PTO or budgets. You are managing the strategy of how fast growing biotech upstarts handle their pivotal health authority submissions.
  • The "Credibility" Factor: You use your dual background (Operator + Consultant) to provide advice that sticks. When a customer says, "That won't work in a global submission," you have the lived experience to show them exactly how it will.
  • Commercial Impact: You aren't just "supporting" sales; you are the secret weapon. You identify market gaps and work directly with Product teams to ensure Veeva remains the industry standard.
What This Job Is NOT
  • NOT People Management: You are an elite individual contributor. Your success is measured by market impact, not headcount.
  • NOT Regulatory Affairs or Science: We aren't developing regulatory strategy for sponsors. We are architecting the systems that manage their deliverables and speed their products to market.
  • We deliver working, transformative technology solutions.
What You'll Do
  • Act as the “CEO of your deal” during the sales cycle for complex deals. You bring together the best of Veeva to propose business capability improvements with tangible business value to senior executives.
  • Serve as the "Face of Veeva Regulatory." You will speak at key conferences such as Veeva Summit and DIA to shape the industry's conversation around RIM AI, IDMP, eCTD, and data governance.
  • Be the voice of the customer for our Product and Engineering teams. You tell them what the industry needs before the industry even knows it needs it.
  • While you have no direct reports, you will lead "by influence," aligning Sales, Marketing, and Services teams to ensure a unified market strategy.
Requirements
  • 5+ years of experience with regulatory submission document authoring, submission publishing / validation / viewing, registration and commitment tracking, and regulatory document archiving
  • 4+ years of experience consulting for the regulatory operations area of a life sciences company
  • 3+ years of experience selling software and/or services to life sciences organizations
  • Proven ability to innovate across business processes and technology solutions
  • Ability to hold strategic conversations with heads of regulatory and IT regarding the regulatory applications and their use within Regulatory execution
  • Understanding of global drug development & regulatory process
  • Ability to travel for customer meetings and presentations
Perks & Benefits
  • Medical, dental, vision, and basic life insurance
  • Flexible PTO and company paid holidays
  • Retirement programs
  • 1% charitable giving program
Compensation
  • Base pay: $125,000 - $300,000
  • The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com.

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