Description

You will lead software implementation projects within life sciences organizations.

Responsibilities

• Lead solution design for implementing and utilizing the Vault Regulatory suite (Vault Registrations, Vault Submissions, Vault Submission Archive, Vault Publishing).
• Configure, prototype, and document content solutions after leading requirements workshops.
• Manage program and project scope, including resource planning and motivating cross-functional teams.
• Serve as the primary customer liaison, managing communication between the project team, customer, and internal stakeholders.
• Mentor project team members 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 (Labeling, Submission Publishing, Viewing systems).
• Expert knowledge of life sciences compliance and computer systems validation requirements.
• Demonstrated ability to collaborate and communicate effectively with diverse stakeholders.
• Experience leading teams through difficult decisions and negotiating compromises.
• Technical ability to design and implement RIM solutions hands-on.
• Ability to work independently in a dynamic environment.
• Experience with Veeva Vault.
• Experience with Parexel, Liquent Insight, CSC Regulatory Tracker, Arisglobal Register, Opentext, Sharepoint, Documentum, Firstpoint, Nextdocs.

Key Skills

Education

Any Graduate