Your Role:
As a Veeva Vault Clinical Specialist (CTMS & eTMF), you will be responsible for implementing, configuring, and managing Veeva Vault Clinical solutions for Life Sciences clients. You will collaborate with business stakeholders, clinical teams, and IT partners to deliver compliant, scalable, and efficient clinical trial management and documentation solutions.

In this role, you will:
- Lead development activities and guide teams across the full project lifecycle, from requirement gathering to deployment.
- Assess current processes, identify improvement areas, and propose technology-driven solutions.
- Ensure compliance with Life Sciences regulatory and domain standards.
- Contribute to support transition activities, including documentation and knowledge transfer.

Your Profile:
Experience:
- 4 to 6 years of total IT experience, with minimum 3 years of hands-on experience in implementing Veeva Vault solutions for Life Sciences clients.
- Solid experience in Veeva Vault Clinical modules:
- CTMS (Clinical Trial Management System):
- eTMF (electronic Trial Master File)




- Good understanding of Veeva Vault platform capabilities and configurations.
- Experience in leading development teams and working with global client stakeholders.
- Ability to drive projects end-to-end across implementation, configuration, and support phases.

Certifications:
- Veeva Certified Associate - Mandatory.

What You’ll Love About Working Here:
- Opportunity to work on leading Veeva Vault Clinical platforms for global Life Sciences clients.
- Exposure to end-to-end clinical solutions and regulated environments.
- Collaborative culture focused on innovation, learning, and growth.

About Capgemini in India:
Capgemini is an AI‑powered global business and technology transformation partner, helping organizations realize their future through technology, data, and people. With nearly 60 years of heritage, Capgemini is a responsible and diverse organization with 420,000 team members across mo

📌 Veeva Clinical (Pune)
🏢 Capgemini
📍 Pune