[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.ResponsibilitiesServe as a functional SME for Veeva Vault RIM and related Clinical/Regulatory business processesLead or support business process discovery, current-state/future-state assessments, and gap analysis workshopsGather, analyze, and document business, functional, and technical requirementsDevelop process maps, workflow designs, user stories, and business rules to support Veeva implementationsPartner with Veeva delivery teams, client stakeholders, and NNIT technical consultants to accelerate project readinessSupport Phase 0 assessments and implementation planning activities, including governance, data readiness, and operating model designAssist with data migration readiness, role and permission matrix development, and validation planningContribute to User Acceptance Testing (UAT), requirements traceability, and solution verification activitiesSupport hypercare and Managed Services engagements by providing functional expertise, issue analysis, and continuous improvement recommendationsHelp develop reusable accelerators, templates, playbooks, and best practices that can be leveraged across multiple client engagementsSkills5+ years of experience in Life Sciences consulting, Regulatory Affairs, Clinical Operations, or Veeva implementation projectsExperience supporting Veeva Vault RIM, eTMF, QMS, or related Vault applicationsFamiliarity with GxP environments and Computer Software Assurance (CSA) or CSV methodologiesExperience working within global delivery models and cross-functional project teamsPrior consulting or Managed Services experience is highly desirableStrong understanding of Clinical Development and/or Regulatory Affairs processes within the Life Sciences industryExperience with Veeva Vault RIM (Registrations, Submissions, Submissions Archive, or Publishing) preferredExperience working with Veeva Vault platform implementations or support engagementsAbility to facilitate workshops and communicate effectively with business and technical stakeholdersExperience documenting business requirements, process flows, user stories, and functional specificationsFamiliarity with data migration, validation, UAT, and change management activitiesUnderstanding of regulatory submissions, product registrations, document management, or end-to-end regulatory operationsStrong analytical, communication, and organizational skills with a consultative mindsetBenefitsCompetitive SalaryMedical, Dental, Vision Insurance401KPaid HolidaysAnnual Paid Time OffCompany OverviewNNIT is an international IT service provider offering IT consultancy and the development, implementation and outsourcing of IT services. It was founded in 1994, and is headquartered in Søborg, Hovedstaden, DNK, with a workforce of 1001-5000 employees. Its website is http://www.nnit.com.Company H1B SponsorshipNNIT has a track record of offering H1B sponsorships, with 3 in 2026, 7 in 2025, 8 in 2024, 21 in 2023, 2 in 2022, 1 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role.