Senior Implementation Consultant - RIMS (Remote)
Veeva Systems5 years ago
London, United KingdomSenior
Responsibilities
- Lead software implementation projects for pharmaceutical, biotechnology, and other life sciences companies
- Lead solution design and deployment for Vault Registrations, Vault Submissions, Vault Submissions Archive, and Vault Publishing
- Lead configuration requirements workshops; design, prototype, configure, and document content solutions
- Manage program and project activities, including resource planning and leading and motivating cross-functional teams
- Act 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/or viewing systems
- Strong collaboration and communication skills with diverse stakeholders and a demonstrated ability to deliver customer satisfaction
- Experience leading teams through difficult decisions and negotiating compromises
- Technical ability and willingness to design and implement regulatory information management solutions 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 similar 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, and/or medical device and diagnostics regulatory processes, data, and content
- PMP certification is preferred
- Agile methodology experience and/or ACP Certification is preferred
- A life science, computer science, or related degree is preferred
- SaaS/cloud experience is preferred
- Fluency in German, French, Spanish, or Italian is preferred
Benefits
- Remote work from home or office as a Work Anywhere company
- Remote position within the EU/UK with no fixed work-location requirement, provided the candidate is near an airport and can meet travel requirements
- 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.