What You'll Do
- Implement software and design solutions with our Veeva Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Submissions Publishing) at life sciences customers
- 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
Requirements
- 3+ years in technology implementation services, in life sciences or healthcare
- 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 work hard in a fast-paced environment
- Ability to travel as required by the business
Nice to Have
- 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
- Fluency in one or more of the following languages: English, German, French, Spanish, Italian
