
Customer Tech-Salesforce-Veeva Manager-GDS02
- Bangalore, Karnataka
- Permanent
- Full-time
- Act as the subject matter expert (SME) for Veeva CTMS, eTMF, and EDC across our Life Sciences consulting projects.
- Lead end-to-end configuration of Veeva CTMS, eTMF, and EDC to support clinical trial planning, execution, data management, and reporting for various clients.
- Manage stakeholder relationships with clients to gather requirements and implement platform enhancements that align with their clinical operation's needs.
- Ensure compliance with regulatory standards and internal processes throughout the clinical trial lifecycle for client projects.
- Collaborate with cross-functional teams (Clinical Operations, Data Management, Regulatory, IT) within client organizations to optimize system usage and streamline workflows.
- Provide training and support to client end-users, ensuring the adoption of Veeva best practices in CTMS, eTMF, and EDC.
- Monitor system performance, troubleshoot issues, and manage vendor relationships to ensure optimal functionality for client implementations.
- Support audits and inspections by maintaining accurate documentation and audit trails for client projects.
- Bachelor's degree in Life Sciences, Information Technology, or related field.
- 6+ years of hands-on experience with Veeva CTMS, eTMF, and EDC in a pharmaceutical or life sciences consulting environment.
- Strong analytical and problem-solving skills.
- Understanding of clinical trial processes, data management, and regulatory compliance.
- Excellent communication, stakeholder management, and problem-solving skills.
- Experience with other clinical trial management systems (CTMS), electronic data capture (EDC) platforms, or electronic trial master files (eTMF).
- Exposure to clinical trial optimization or digital transformation initiatives within consulting.
- Veeva certifications (CTMS, eTMF, EDC) are a plus.