
Urgent: Clinical Veeva Vault Subject Matter Expert
4 weeks ago
6-months contract.
Responsibilities
- Serve as the primary technical expert for Veeva Clinical CTMS, eTMF, and CDMS systems.
- Lead the implementation, configuration, and maintenance of Veeva systems to support clinical trials and operations.
- Collaborate with cross-functional teams including Clinical Operations, IT, and external vendors to ensure system alignment with business needs.
- Provide technical guidance and support for system integrations, data migrations, and upgrades.
- Develop and maintain system documentation, including technical specifications, user guides, and SOPs.
- Troubleshoot and resolve technical issues related to Veeva systems, ensuring minimal disruption to clinical operations.
- Conduct training sessions and workshops for end-users to enhance system utilization and efficiency.
- Stay current with industry trends and advancements in clinical systems and technology to recommend improvements and innovations.
- Ensure compliance with regulatory requirements and company policies in all system-related activities.
Requirements
- Bachelor's degree in Computer Science, Information Technology, Life Sciences, or a related field. Advanced degree preferred.
- Minimum of 7-10 years of experience in a technical role supporting clinical systems, with at least 5 years specifically working with Veeva Clinical CTMS, eTMF, and CDMS.
- Strong understanding of clinical trial processes and regulatory requirements.
- Proven experience in system implementation, configuration, and maintenance.
- Excellent problem-solving skills and the ability to troubleshoot complex technical issues.
- Strong communication and interpersonal skills, with the ability to work effectively with diverse teams.
- Experience with system integrations, data migrations, and upgrades.
- Ability to manage multiple projects and priorities in a fast-paced environment.
- Certification in Veeva systems is mandatory.
- Technical Skills:
- Proficiency in Veeva Clinical CTMS, eTMF, and CDMS systems.
- Knowledge of SQL, database management, and data analysis.
- Familiarity with clinical data standards (e.g., CDISC, SDTM).
- Experience with cloud-based solutions and SaaS platforms.
- Understanding of GxP, 21 CFR Part 11, and other regulatory requirements.
- Statistical analysis tools SAS server, PC SAS, R studio, Qlik, CDISC tools Pinnacle 21, RYZE experience is a plus.
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