PV senior level

Responsible for end-to-end pharmacoangiograp operations, global safety data management across clinical trials.

Your new company

Global helthcare company
End-to-end clinical development support
Collaborative & inclusive culture
Fully remote work environment

Your new role

Safety Management Plan authoring
SAE review / data entry / QC activities
Regulatory reporting & periodic safety reports
Investigator Meeting participation
Query handling & site follow-up
Global team collaboration

What you'll need to succeed

5+ years PV experience (clinical trials)
Strong knowledge of AE/SAE processing
GCP & PV regulations understanding
Fluent English (written & spoken)
Safety database experience (e.g. Argus preferred)
Strong multitasking & time management

What you'll get in return

Fully remote working style
Involvement in global projects
Exposure to multiple therapeutic areas
Flexible work culture

What you need to do now


If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Inner Tokyo
Specialism
Life Sciences
Ref:
1129363
Closing date
30 Jun 2026

Talk to a consultant

Talk to Maya Taguchi, the specialist consultant managing this position, located in Tokyo Head Office
Izumi Garden Tower 38th Floor, 1-6-1 Roppongi

Telephone: +810345655908

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