Director – Veeva Regulatory

Job not on LinkedIn

🕒 October 31, 2025

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $125k - $300k / year

⏰ Full Time

🔴 Lead

🚔 Compliance

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 21%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Veeva Systems

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Veeva Systems is a cloud-computing company focused on the global life sciences industry. It provides software, data, and consulting services to streamline research and development, quality management, regulatory operations, and commercial processes. Veeva's solutions encompass clinical trials, regulatory submissions, drug safety management, and commercial execution to support life sciences enterprises in their mission to improve and extend life.

📋 Description

• Responsible for growing and sustaining the Regulatory market for the Veeva RIM applications including Vault Registrations, Submissions, Submissions Archive, and Submissions Publishing • Provide thought leadership and sales support to teams in driving new opportunities in the Regulatory space • Provide business and technology guidance to the product team in support of new or enhanced features and functionality in regulatory applications • Develop strategy and messaging for customer adoption of new features and functionality for new and existing customer base • Sales & Consulting • Coordinate resources across the customer lifecycle from sales to delivery and beyond • Present at industry conferences, leading webinars and authoring articles for industry publications

🎯 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

🏖️ Benefits

• Medical, dental, vision, and basic life insurance • Flexible PTO and company paid holidays • Retirement programs • 1% charitable giving program