[Remote] Senior Consultant- Clinical & Regulatory Information Management

Note: The job is a remote job and is open to candidates in USA. NNIT is a public listed company specializing in IT solutions for life sciences internationally. They are seeking a highly motivated Clinical / Regulatory Information Management Subject Matter Expert to support and expand their Veeva Technology Practice, serving as a cross-functional resource for multiple client deliveries.

Responsibilities

• Serve as a functional SME for Veeva Vault RIM and related Clinical/Regulatory business processes
• Lead or support business process discovery, current-state/future-state assessments, and gap analysis workshops
• Gather, analyze, and document business, functional, and technical requirements
• Develop process maps, workflow designs, user stories, and business rules to support Veeva implementations
• Partner with Veeva delivery teams, client stakeholders, and NNIT technical consultants to accelerate project readiness
• Support Phase 0 assessments and implementation planning activities, including governance, data readiness, and operating model design
• Assist with data migration readiness, role and permission matrix development, and validation planning
• Contribute to User Acceptance Testing (UAT), requirements traceability, and solution verification activities
• Support hypercare and Managed Services engagements by providing functional expertise, issue analysis, and continuous improvement recommendations
• Help develop reusable accelerators, templates, playbooks, and best practices that can be leveraged across multiple client engagements

Skills

• 5+ years of experience in Life Sciences consulting, Regulatory Affairs, Clinical Operations, or Veeva implementation projects
• Experience supporting Veeva Vault RIM, eTMF, QMS, or related Vault applications
• Familiarity with GxP environments and Computer Software Assurance (CSA) or CSV methodologies
• Experience working within global delivery models and cross-functional project teams
• Prior consulting or Managed Services experience is highly desirable
• Strong understanding of Clinical Development and/or Regulatory Affairs processes within the Life Sciences industry
• Experience with Veeva Vault RIM (Registrations, Submissions, Submissions Archive, or Publishing) preferred
• Experience working with Veeva Vault platform implementations or support engagements
• Ability to facilitate workshops and communicate effectively with business and technical stakeholders
• Experience documenting business requirements, process flows, user stories, and functional specifications
• Familiarity with data migration, validation, UAT, and change management activities
• Understanding of regulatory submissions, product registrations, document management, or end-to-end regulatory operations
• Strong analytical, communication, and organizational skills with a consultative mindset

Benefits

• Competitive Salary
• Medical, Dental, Vision Insurance
• 401K
• Paid Holidays
• Annual Paid Time Off

Company Overview

Company H1B Sponsorship