Senior Consultant - Veeva Vault Safety - Japan & PMDA
Veeva Systems (company site, opens in a new tab)10+ yrsRemoteDirect career pageEst. 25–45 LPA
Posted on 2 Sept
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Job description
Structured overview of role & requirements
About This Role
- Lead business workshops to gather and clarify requirements for implementing Veeva Safety on the Veeva cloud platform supporting biopharmaceutical customers.
- Design and deliver solutions including configuration oversight, data migration advisory, and change management for transitioning customers from on-premises to SaaS.
- Act as liaison between customers, internal product teams, and consultants to ensure successful Vault Safety implementation and customer adoption.
Minimum Requirements
- 10+ years of life sciences experience, majority in Drug Safety and Pharmacovigilance, including consulting experience.
- Strong knowledge of Japan Green Book and PMDA safety reporting requirements.
- Experience with safety systems implementation (e.g., Aris, Argus, Emperica, Commonwealth, RxLogix) and SQL query writing on safety data sets.
- Bachelor’s degree or equivalent; Japanese language proficiency preferred but not strictly mandatory.
Ideal Candidate Profile
- Experienced individual contributor with deep domain expertise in Drug Safety and Pharmacovigilance in life sciences, especially in Japanese regulatory context.
- Proven ability to lead workshops and communicate effectively with diverse stakeholders including Japanese-speaking customers and global teams.
- Comfortable working hands-on in solution design, problem solving, and change management within SaaS implementations for life sciences safety solutions.