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AbbVie Inc.: Senior Associate or Manager, RA TA Group, Regulatory Affairs(Neurology)

Observed on the employer’s careers system, last checked 2026-09-11.

POSTED: 2026-08-05Listed

Cite: FACTANKER, https://factanker.com/jobs/posting/03b91b03-0f74-487f-9240-27f6720708b2

Employer
AbbVie Inc.
Location
Minato City
Category
Other
Posted
2026-08-05
Careers system
smartrecruiters
Observed
2026-09-11

Apply on the employer’s site ↗

Role description

Verbatim from the employer’s posting, rendered as plain text.

Summary of Job Description: Manager, Regulatory Affairs (RA) Therapeutic Area (TA) Group, Regulatory Affairs Japan, is accountable for executing regulatory activities within assigned projects or therapeutic areas, acting as a core member of project teams. This role ensures timely and high-quality regulatory deliverables, supports regulatory strategy, and maintains compliance with applicable regulations and company policies. The Manager proactively collaborates with internal and external stakeholders and contributes to the continuous improvement of regulatory processes. Major Responsibilities: Execute regulatory affairs activities for assigned projects, including preparation and submission of regulatory documents (e.g., New Drug Applications, PMDA consultations, Clinical Trial Notifications, package inserts) to PMDA/MHLW. Collaborate with cross-functional project teams (e.g., Clinical…

Provenance

Official posting
https://jobs.smartrecruiters.com/AbbVie/3743990014443106
Retrieved
2026-09-11 10:30:47.489871+02:00
ATS reference
3743990014443106