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Veeva Systems, a $3B+ SaaS leader in life sciences cloud, seeks a Senior Consultant specializing in Drug Safety and Pharmacovigilance to join its Professional Services team. You will support biopharmaceutical customers implementing Veeva Vault Safety on Veeva's development cloud platform, acting as a trusted subject matter expert and customer liaison.
Key responsibilities include leading business workshops to gather and document functional/non-functional requirements; designing solutions that address both stated and latent customer needs; collaborating with configuration teams to develop implementations; managing communication between implementation teams, customer stakeholders, and Veeva product teams; advising on data migration activities; guiding customers in adopting Vault and industry best practices; and driving change management for transitions from on-premises to SaaS solutions.
You must bring 10+ years of life sciences industry experience, with the majority in Drug Safety and Pharmacovigilance consulting. Japanese language proficiency is preferred, with strong understanding of Japan Green Book and PMDA safety reporting requirements. Required skills include conducting/supporting workshops, deep knowledge of drug safety processes and regulations, complex SQL query writing on safety datasets, and hands-on experience implementing safety systems (Aris, Argus, Emperica, Commonwealth, RxLogix, or proprietary platforms). You should demonstrate proven ability to collaborate across diverse stakeholders, strong English communication (written and verbal), and a track record of individual contributor work. Additional assets include JLPT N2/N1 certification, experience with Argus, SQL/PLSQL programming, life science degree, SaaS/cloud exposure, and services delivery management background. Travel (~25% project time) required. Bachelor's degree or equivalent mandatory.
