IN_Senior Associate_Veeva RIM Consultant_Enterprise Apps-SFDC_Advisory_ Bangalore
PwC IndiaMatch Score
Against your primary resumeLogin to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Protocol Intelligence
Data-driven signals on your job's competitivenessLog in to see why each signal reads the way it does.
Job Description
Structured overview of role & requirementsAbout This Role
Configure and implement Veeva Vault RIM applications including Registrations, Submissions, Submissions Archive, and Publishing for global life sciences clients.
Gather business requirements, conduct workshops with regulatory stakeholders, and prepare functional design documents to support regulatory affairs transformation initiatives.
Support system testing, validation, deployment, release management, post-production activities, and collaborate on integrations and data migration ensuring compliance with GxP, FDA, EMA, and global regulatory standards.
Minimum Requirements
4 to 7 years of IT/Consulting experience with minimum 2 to 3 years hands-on in Veeva Vault RIM implementation and support.
Bachelor's degree in Engineering, Pharmacy, Life Sciences, or related field.
Experience in Veeva Vault configuration, workflows, security, document management, and understanding of Regulatory Affairs processes and submission management.
Knowledge of SDLC, Agile methodology, and validation processes is required.
Ideal Candidate Profile
Experienced in working with global regulatory teams and life sciences domain clients specifically on regulatory information management.
Possesses strong analytical, communication, stakeholder management skills, and can engage effectively with multi-disciplinary technical and regulatory teams.
Familiar with digital transformation projects in compliance-heavy environments, with ability to handle configurations, integrations, and documentation effectively.