Implementation Consultant RIM
Veeva Systemsover 1 year ago
Barcelona, SpainMid Level
Responsibilities
- Implement and design solutions using the Veeva Regulatory suite for life sciences customers.
- Lead requirements workshops, solution design and documentation, prototyping, and solution deployment.
- Manage program and project activities, including resource planning and leading and motivating cross-functional teams.
- Coordinate communication among the project team, 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, and organizational skills.
- Ability to work effectively with diverse stakeholders in a fast-paced environment.
- 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 one or more of English, German, French, Spanish, or Italian is preferred.
Benefits
- Work Anywhere flexibility with remote or office options
- Remote position within the EU/UK for candidates near an airport who can meet travel requirements
- Travel required as needed by the business
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.