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Strong employer brand and remote role but senior, niche Drug Safety and PMDA expertise reduces applicant density.
Highly domain-specific drug safety, PMDA and Japanese language requirements limit cross-industry transferability.
Explicit 10+ years, domain expertise, SQL and specific safety-system experience make filters stringent.
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.
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.
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.