Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Consultant - Veeva Rim Professional Services

Veeva Systems
3+ years
Not Disclosed
Bangalore, Hyderabad, Mumbai, India
1 June 5, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Consultant – Veeva RIM Professional Services

Company: Veeva Systems
Role: Consultant – Veeva RIM Professional Services
Department: Professional Services
Location: Mumbai, Hyderabad, Bengaluru, Pune (Remote/Work Anywhere)
Employment Type: Full-Time, Permanent
Experience Required: 3+ Years
Travel Requirement: 25%–50%


Role Overview

The Consultant – Veeva RIM Professional Services is responsible for helping pharmaceutical, biotechnology, and life sciences organizations modernize and optimize their Regulatory Information Management (RIM) processes through implementation of Veeva's regulatory technology solutions.

This is a client-facing consulting role that combines Regulatory Affairs/Regulatory Operations expertise, business process consulting, solution design, project management, and system implementation.

You will work closely with global regulatory teams to understand business requirements, configure Veeva applications, and drive successful digital transformation initiatives.


Key Responsibilities

Regulatory Solution Consulting

  • Analyze customer regulatory business processes and requirements.

  • Recommend best practices for regulatory information management.

  • Translate business requirements into system configurations and solution designs.

  • Support digital transformation initiatives within Regulatory Affairs organizations.

Veeva RIM Implementation

Configure and implement:

  • Veeva Registrations

  • Veeva Submissions

  • Veeva Submissions Archive

  • Veeva Publishing

Key activities include:

  • System configuration

  • Workflow setup

  • Business process mapping

  • User acceptance support

  • Deployment activities

Workshop & Requirements Management

  • Lead customer discovery sessions and workshops.

  • Gather and document business requirements.

  • Conduct fit-gap analysis.

  • Develop solution design documentation.

  • Demonstrate prototypes and proposed solutions.

Project Management

  • Support implementation projects from initiation through go-live.

  • Assist in project planning and resource allocation.

  • Track deliverables and milestones.

  • Coordinate activities across multiple stakeholders.

Stakeholder Communication

  • Act as liaison between:

    • Regulatory teams

    • Business users

    • IT teams

    • Project managers

    • Veeva internal teams

  • Present solutions and implementation updates to customers.


Required Qualifications

Experience

  • 3+ years of experience in:

    • Regulatory Affairs

    • Regulatory Operations

    • Life Sciences Consulting

    • Healthcare Technology Consulting

    • Pharmaceutical IT Systems

    • RIM-related projects

Technical Skills

  • Ability to configure and implement enterprise software solutions.

  • Strong business process analysis skills.

  • Understanding of cloud-based software implementations.

  • Experience gathering and documenting requirements.

Core Competencies

  • Client-facing communication

  • Consulting mindset

  • Project coordination

  • Problem solving

  • Stakeholder management

  • Team collaboration

  • Organizational skills


Preferred Qualifications

Regulatory Expertise

Knowledge of:

  • Regulatory Affairs

  • Regulatory Operations

  • Global submission management

  • Regulatory publishing

  • Submission archiving

  • Product registrations

Industry Knowledge

Understanding of:

  • Drug development lifecycle

  • Pharmaceutical compliance requirements

  • Regulatory submission processes

  • Global health authority interactions

Validation & Compliance

Experience with:

  • Computer System Validation (CSV)

  • GxP compliance

  • Life sciences quality systems

Consulting Background

Experience working with:

  • Software vendors

  • System integrators

  • Digital transformation projects

  • Enterprise software implementation teams