Implementation Consultant RIM
Veeva Systemsover 1 year ago
London, United KingdomMid Level
Responsibilities
- Implement software and design solutions using the Veeva Regulatory suite for life sciences customers.
- Lead configuration requirements workshops and design, document, prototype, and deploy solutions.
- Manage programs and projects, including resource planning and leading and motivating cross-functional teams.
- Communicate among project teams, customers, and internal stakeholders.
Requirements
- At least 2 years of experience as a consultant, business representative, or IT representative.
- Technical ability and willingness to design and implement a regulatory information management solution hands-on.
- Strong collaboration, communication, organization, and stakeholder management skills.
- Ability to travel as required by the business.
- Consulting experience with a major system integrator or software vendor is preferred.
- Knowledge of drug development, Regulatory Affairs, or Regulatory Operations is preferred.
- Experience with life sciences compliance and computer systems validation requirements is preferred.
- Fluency in English, German, French, Spanish, Italian, or another listed language is preferred.
Benefits
- Work Anywhere arrangement with the option to work remotely or from an office.
- Remote position within the EU/UK for candidates near an airport who can meet travel requirements.
- Opportunity to work with life sciences customers and Veeva’s Professional Services team.
Categories
Solutions Engineering
About Veeva Systems
Veeva Systems builds cloud software and data products for life sciences, including Veeva CRM and the Veeva Vault suite for clinical, regulatory, and quality operations. It sells subscriptions and services to biopharma and related companies to manage R&D, compliance, and commercial workflows. Founded in 2007 and headquartered in Pleasanton, California, Veeva is publicly traded on the NYSE and has operated as a Public Benefit Corporation since 2021.