Contract role: Veeva Vault Clinical Lead at Branchburg, NJ (Onsite from day 1)

Veeva Vault Clinical Lead

Branchburg, NJ (Onsite from day 1)

Long Term Contract

Core responsibilities

• System Configuration: Set up and configure Veeva Vault applications, such as CDMS (for data management) or CTMS (for trial management). This includes configuring forms, edit checks, workflows, and roles.
• Clinical Processes: Apply a strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements to configure the system to meet business needs.
• User Support: Provide L2 or L3 support, troubleshoot issues, and manage change requests and enhancements for the Veeva Vault applications.
• Validation & Compliance: Lead and support validation activities, including creating validation documentation and ensuring the system is compliant with regulations like GxP and 21 CFR Part 11.
• Integration & Migration: Assist with integrating Veeva Vault with other clinical systems and support data migration activities from legacy systems.
• Training: Provide training and support to clinical and operational users to ensure effective system adoption.
• Required skills and experience
• Veeva Vault Expertise: Hands-on experience with specific Veeva Vault modules like CTMS, eTMF, CDMS, Study Startup, or others.
• Clinical Knowledge: Deep understanding of the clinical development lifecycle and trial processes.
• Technical Skills: Experience with system configuration, data management principles, and potentially APIs, Vault APIs, or the Vault Java SDK.
• Regulatory Knowledge: Familiarity with GxP, GCP, and other relevant regulatory guidelines.
• Soft Skills: Excellent communication, problem-solving, analytical skills, and stakeholder management.
• Certifications: Relevant Veeva Vault certifications are often a plus or sometimes mandatory.
• Other Tools: Experience with tools like Jira, ServiceNow, or other ticketing and project management systems is frequently mentioned.