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Veeva

Posted 3 months ago

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Consultant - Veeva RIM Professional Services

HyderabadRemoteFull-time

AI Summary

Consultant in Veeva's Professional Services team guiding life science customers to configure and implement Veeva's Regulatory suite (RIM, submission management, publishing, archiving), leading requirements workshops, solution design, and deployment.

About this role

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.
At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Veeva is looking for Consultants with deep regulatory expertise and a passion for helping customers improve their process for Regulatory Information Management (RIM), submission management, publishing, and submission archiving. We want team members ready to challenge the status quo; you’re ready to transform businesses.
As a member of our Professional Services team, you will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and configuring our cloud-based solution for managing regulatory information across the enterprise.
This is a remote, full-time permanent role with Veeva with a location preference in Hyderabad, Mumbai, Bengaluru, or Pune.

What You'll Do

  • Guide life science customers in the configuration and implementation of Veeva’s Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes
  • Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions
  • Program and project management, including resource planning, leading and motivating a cross-functional team
  • Communicate between the project team, customer, and internal stakeholders

    • Requirements

  • 3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative
  • Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution
  • Ability to collaborate and communicate excellently with diverse stakeholders
  • Team player with strong organization skills and an ability to act with speed in a complex environment
  • Ability to travel (25% -50%) as required by the business

    • Nice to Have

  • Consulting experience, working with a major system integrator or software vendor
  • Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
  • Experience in life sciences compliance and computer systems validation requirements

    • Perks & Benefits

  • Health and wellness programs
  • Life Assurance
  • Veeva charitable giving program
  • Additional annual leave over Christmas break

    • Skills

    ComplianceHealthcareLife SciencesRegulatory Information Management (RIM)Submission ArchivingSubmission ManagementVeeva PublishingVeeva RegistrationsVeeva SubmissionsVeeva Submissions Archive

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