RIM Implementation Consultant

Summary

Veeva Systems is a mission-driven pioneer in industry cloud software for the life sciences industry. The RIM Implementation Consultant will help customers optimize regulatory data and document management processes by translating global regulatory needs into solution designs and configuring Veeva’s cloud-based regulatory information management solutions. The role also involves leading workshops, managing projects, and coordinating communication among project teams, customers, and internal stakeholders.

Responsibilities

• Guide life science customers in the configuration and implementation of Veeva’s Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes
• Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions
• Program and project management, including resource planning, leading and motivating a cross-functional team
• Communicate between the project team, customer, and internal stakeholders

Skills

• - 3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative
• - Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution
• - Ability to collaborate and communicate excellently with diverse stakeholders
• - Team player with strong organization skills and an ability to act with speed in a complex environment
• - Ability to travel as required by the business
• - Consulting experience, working with a major system integrator or software vendor
• - Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
• - Experience in life sciences compliance and computer systems validation requirements

Qualifications

Must Haves

• - 3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative
• - Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution
• - Ability to collaborate and communicate excellently with diverse stakeholders
• - Team player with strong organization skills and an ability to act with speed in a complex environment
• - Ability to travel as required by the business

Nice to Haves

• - Consulting experience, working with a major system integrator or software vendor
• - Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
• - Experience in life sciences compliance and computer systems validation requirements

Benefits

• Work Anywhere flexibility to work from home or in the office
• Medical, dental, vision, and basic life insurance
• Flexible PTO and company paid holidays
• Retirement programs
• 1% charitable giving program
• May be eligible for variable bonus and/or stock bonus