Veeva RIM Expert

You will lead software implementation projects within life sciences organizations.

Responsibilities

• Lead solution design for the implementation and use of the Vault Regulatory suite (Vault Registrations, Vault Submissions, Vault Submission Archive, Vault Publishing).
• Configure, prototype, and document content solutions following requirements workshops.
• Manage program and projects, including resource planning and leading cross-functional teams.
• Serve as the primary customer liaison, managing communication between the project team, customer, and internal stakeholders.
• Mentor project teams and consultants to improve consulting skills.

Required Skills

• 8+ years of system implementation experience in life sciences or healthcare (consultant, business, or IT representative).
• In-depth knowledge of drug development processes and regulatory submissions, including Labeling, Submission Publishing, and Viewing systems.
• Expertise in life sciences compliance and computer systems validation requirements.
• Technical ability to design and implement a RIM solution while being willing to execute hands-on tasks.
• Proven ability to communicate and collaborate with diverse stakeholders to ensure high satisfaction.
• Experience leading teams through complex decisions and negotiating compromises.
• Ability to work independently in a dynamic environment.
• Familiarity with Rim Suite and Vault Regulatory Suite.
• Experience with systems like Insight, Csc Regulatory Tracker, Arisglobal Register, Opentext, Sharepoint, Documentum, and Firstdoc.