CareerPlan

CRA I, CRA II and Senior CRA

Japan, TokyoFull-time2026-11-09 → 2026-11-10

Core

Clinical trial monitoring and study setup coordination to ensure patient safety and regulatory compliance.

Role type

Clinical Research Associate (CRA)

Builds

Clinical trial operations and study monitoring deliverables

Domain

Healthcare / Clinical Research

Deliverable

client delivery

Required skills

Clinical trial monitoring, ICH-GCP guidelines, medical data review, study documentation management, stakeholder relationship management, query resolution

Preferred skills

None stated

Technologies

None stated

Responsibilities

Coordinate study setup and monitoring activities, complete study status reports, maintain study documentation, run sponsor queries, ensure compliance with procedures and protocols

Seniority

Entry to Senior level (CRA I, II, Senior)