Senior Implementation Consultant - RIMS (Remote)
Veeva Systemsover 1 year ago
Barcelona, SpainSenior
Responsibilities
- Lead software implementation projects for life sciences companies.
- Lead solution design and implementation of Vault Registrations, Vault Submissions, Vault Submissions Archive, and Vault Publishing.
- Lead configuration requirements workshops; design, prototype, configure, and document content solutions.
- Manage programs and projects, including resource planning and leadership of cross-functional teams.
- Serve as the primary customer liaison between the project team, customer, and internal stakeholders.
- Mentor project team members and consultants to improve consulting skills.
Requirements
- 8+ years of system implementation experience with life sciences or healthcare companies, either as a consultant, business representative, or IT representative.
- In-depth knowledge of drug development processes and regulatory submissions, including labeling, submission publishing, and viewing systems.
- Ability to collaborate and communicate with diverse stakeholders while delivering high customer satisfaction.
- Experience leading teams through difficult decisions and negotiating compromises.
- Technical ability and willingness to design and implement a regulatory information management solution hands-on.
- Expertise in life sciences compliance and computer systems validation requirements.
- Ability to work independently in a fast-paced environment.
- Ability to travel as required by the business.
- Preferred experience with Veeva Vault, PAREXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, or other regulatory information management and submission publishing systems.
- Preferred consulting experience with a major system integrator or software vendor.
- Preferred background in Regulatory Affairs, Regulatory Operations, or Pharmacovigilance.
- Preferred knowledge of pharmaceutical, biotechnology, medical device, and diagnostics regulatory processes, data, and content.
- PMP certification, Agile execution experience or ACP certification, SaaS/cloud experience, and fluency in German, French, Spanish, or Italian are preferred.
- A life science, computer science, or related degree is preferred.
Benefits
- Remote work within the EU/UK with no fixed work location requirement, subject to proximity to an airport and travel requirements.
- Work Anywhere flexibility to work from home or in the office.
- Travel as required 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.