Accenture is currently hiring a Specialist – Veeva Vault / Regulatory Information Management (RIM) professional with 1–3 years of experience. This opportunity is ideal for candidates with expertise in Veeva Vault platform, regulatory submissions, and regulatory information management systems.
Professionals with experience in Veeva Vault workflows, document lifecycle management, and regulatory data integrity will have an excellent opportunity to work on global regulatory processes within a leading consulting and technology services organization.
This role focuses on supporting Regulatory Information Management (RIM) processes, managing Veeva Vault workflows, and ensuring compliance with regulatory documentation standards used across global pharmaceutical and life sciences organizations.
Job Details
| Field | Details |
|---|---|
| Job Title | Specialist – Veeva Vault / RIM |
| Company | Accenture |
| Experience | 1–3 Years |
| Industry | Pharmaceutical / Life Sciences / Regulatory Affairs |
| Employment Type | Full-Time |
| Joining | Immediate Joiners Preferred |
Key Responsibilities
The selected candidate will support Veeva Vault Regulatory Information Management processes and ensure proper workflow execution within the regulatory ecosystem.
Key responsibilities include:
- Manage Veeva Vault document lifecycle processes, including review, approval, and archival.
- Support Regulatory Information Management (RIM) activities for regulatory submissions and registrations.
- Maintain data integrity, metadata accuracy, and document control within the Veeva Vault system.
- Coordinate with cross-functional regulatory teams to ensure timely submission preparation and documentation management.
- Monitor and maintain regulatory workflows, submissions tracking, and health authority interactions.
- Ensure regulatory documentation complies with global regulatory standards and internal SOPs.
- Assist in troubleshooting Vault workflow issues, access control, and document configuration.
Required Qualifications
Candidates applying for this Veeva Vault Specialist job should possess the following qualifications:
Education
- Bachelor’s or Master’s degree in:
- Pharmacy (B.Pharm / M.Pharm)
- Life Sciences
- Biotechnology
- Related scientific discipline
Experience
- 1–3 years of experience working with Veeva Vault or Veeva RIM platforms.
Technical Skills
- Strong understanding of Veeva Vault document management and workflows
- Experience with regulatory submissions and registrations
- Familiarity with health authority documentation processes
- Knowledge of regulatory information management systems
Preferred Qualification
- Veeva Vault Certification (highly preferred)
Why Join Accenture?
Working with Accenture Life Sciences and Regulatory Technology teams offers exposure to global regulatory operations and digital regulatory transformation.
Key benefits include:
- Opportunity to work with global pharmaceutical clients
- Exposure to advanced regulatory technology platforms
- Career growth in Regulatory Affairs and Veeva Vault ecosystem
- Collaborative environment with cross-functional regulatory teams
- Competitive salary and professional development opportunities
Salary Estimate
Based on market benchmarks for Veeva Vault / Regulatory Affairs roles in India:
Estimated Salary Range:
₹6,00,000 – ₹10,00,000 per year (depending on experience and certification)
How to Apply
Interested and eligible candidates can apply by sharing their resume directly via email.
Send your resume to:
📧 nalini.shukla@accenture.com
Candidates with immediate availability and Veeva Vault experience are strongly encouraged to apply.