Description

You will lead software implementation projects for life sciences organizations, focusing on the Vault Regulatory suite.

This role is remote.

Responsibilities

• Lead solution design for Vault Registrations, Submissions, Submission Archive, and Publishing.
• Configure, prototype, and document content solutions based on requirements workshops.
• Manage program resources, project timelines, and 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.
• In-depth knowledge of drug development processes and regulatory submissions, including Labeling and Submission Publishing.
• Expertise in life sciences compliance and computer systems validation requirements.
• Technical ability to design and implement RIM solutions with hands-on execution.
• Familiarity with RIM Suite and Vault Regulatory Suite.
• Experience with systems like Insight, CSC Regulatory Tracker, Arisglobal Register, OpenText, SharePoint, Documentum, and Firstdoc.
• Proven ability to communicate and collaborate with diverse stakeholders.

Preferred Skills

• Experience leading teams through complex decisions and negotiating compromises.
• Ability to work independently in a dynamic environment.

Key Skills

Education

Any Graduate