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
Understand customers’ global regulatory needs, translate requirements into solution design, and configure cloud-based RIM solution across the enterprise
Travel as required and support customers globally
Requirements
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 (Nice to Have)
Knowledge of drug development, Regulatory Affairs, or Regulatory Operations (Nice to Have)
Experience in life sciences compliance and computer systems validation requirements (Nice to Have)
Benefits
Medical, dental, vision, and basic life insurance
Flexible PTO and company paid holidays
Retirement programs
1% charitable giving program
Work Anywhere (flexibility to work from home or in the office)
ATS Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.