
Senior Implementation Consultant – RIMS
Posted May 23

Posted May 23
This is a fully remote position, open to applicants in Denmark.
• Oversee software implementation initiatives for life sciences organizations, ranging from major pharmaceutical corporations to budding biotechs.
• Direct the solution design for the deployment and utilization of the Vault Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing).
• Facilitate configuration requirement workshops, design, prototype, configure, and document content solutions.
• Manage programs and projects, including resource allocation, while leading and inspiring a cross-functional team.
• Serve as the primary customer liaison, orchestrating communication among the project team, client, and internal stakeholders.
• Guide project teams and consultants, aiding in the enhancement of their consulting expertise.
• 8+ years of experience in system implementations for life sciences or healthcare sectors, whether in a consulting role or as a business or IT representative.
• Comprehensive understanding of drug development processes and regulatory submissions, encompassing Labeling, Submission Publishing, and/or Viewing systems.
• Demonstrated ability to effectively collaborate and communicate with a variety of stakeholders, ensuring high levels of satisfaction in delivery.
• Influential leader with experience guiding teams through challenging decisions and mediating compromises.
• Technical proficiency and readiness to actively engage in the design, configuration, and implementation of a RIM solution.
• Expert knowledge of life sciences compliance and computer systems validation requirements.
• Capability to work autonomously in a fast-paced environment.
• Willingness to travel as business needs dictate.
• Work Anywhere company, promoting flexibility to work from home or the office.
Strada
Aliz
Strada
Wingman Group
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