Veeva RIM Consultant

About the role

We are seeking an experienced Veeva RIM Consultant to support regulatory data remediation and Veeva RIM initiatives for a leading pharmaceutical client. The ideal candidate will have strong expertise in Veeva RIM, regulatory information management, and data quality, along with experience supporting digital transformation and automation initiatives within a regulated life sciences environment.

Responsibilities

• Perform regulatory data remediation activities within Veeva RIM.
• Configure, maintain, and support Veeva RIM applications.
• Support regulatory information management processes and system enhancements.
• Collaborate with cross-functional teams to improve regulatory data quality and compliance.
• Assist with Veeva RIM reporting, dashboards, and KPI development.
• Support integrations between Veeva Quality and Veeva RIM.
• Participate in SDLC activities, including requirements gathering, testing, and deployment.
• Contribute to AI and automation initiatives to streamline regulatory processes.
• Ensure compliance with regulatory standards and documentation requirements.

Required Qualifications

• Strong hands-on experience with Veeva RIM (Required).
• Experience performing regulatory data remediation.
• Knowledge of IDMP and Pharmacovigilance Management System (PMS) (Required).
• Experience with eCTD submissions and regulatory publishing.
• Understanding of Software Development Life Cycle (SDLC).
• Experience with AI and process automation initiatives.
• Knowledge of integrations between Veeva Quality and Veeva RIM.
• Experience creating and analyzing Veeva RIM reports and KPIs.
• Experience working in a regulated pharmaceutical or biotechnology environment.
• Excellent analytical, communication, and cross-functional collaboration skills.