Customer Tech-Salesforce-Proactive-Veeva Senior-GDS02

At EY, you will be part of a team dedicated to shaping your future with confidence, succeeding in a globally connected powerhouse of diverse teams, and advancing your career to new heights. Join EY and contribute to building a better working world. As a Veeva CTMS Subject Matter Expert (SME) at our consulting firm, you will play a crucial role in supporting our Life Sciences clients by optimizing their clinical trial management processes. Your responsibilities will include managing Veeva CTMS, eTMF, and EDC implementations, ensuring compliance, and facilitating efficient trial lifecycle management for our clients. Key Responsibilities: - Serve as the subject matter expert (SME) for Veeva CTMS, eTMF, and EDC in Life Sciences consulting projects. - Lead the end-to-end configuration of Veeva CTMS, eTMF, and EDC to support various aspects of clinical trial planning, execution, data management, and reporting. - Establish and maintain stakeholder relationships with clients to gather requirements and implement platform enhancements aligned with their clinical operations needs. - Ensure compliance with regulatory standards and internal processes throughout the clinical trial lifecycle for client projects. - Collaborate with cross-functional teams within client organizations to optimize system usage and streamline workflows. - Provide training and support to client end-users to ensure the adoption of 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. Qualifications: - Bachelor's degree in Life Sciences, Information Technology, or a related field. - 3-6 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. Nice to Have: - 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. At EY, we are dedicated to building a better working world by creating new value for our clients, people, society, and the planet. With the help of data, AI, and advanced technology, our teams work to shape the future with confidence and address the most pressing issues of today and tomorrow. Join our globally connected network and diverse ecosystem partners to provide services in over 150 countries and territories.,