Summary
Join Veeva Systems, a leading life sciences industry cloud company, as a Professional Services team member. You will implement and design solutions using Veeva's Regulatory suite, lead configuration workshops, manage projects, and communicate effectively with diverse stakeholders. This remote position within the EU/UK requires experience in consulting, system implementation, and a passion for optimizing regulatory data and document management. The role demands strong technical abilities, excellent communication skills, and the ability to travel as needed. Veeva offers a flexible work environment and is committed to fostering a diverse and inclusive workplace.
Requirements
- 2+ years experience either as a consultant, business, or IT representative
- Technical abilities and willingness to βroll up your sleevesβ to design 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
Responsibilities
- Implement software and design solutions with our Veeva Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva 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
Preferred Qualifications
- 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
Benefits
Work from home or in the office
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