Pharmacovigilance / Data QC Specialist

■担当業務

医薬品安全性情報管理プロジェクトのメンバーとして、副作用情報などの入力内容に対する QCチェックを行う。

■勤務地
品川シーサイド/新大阪

■候補者の要件

■■必須

* 国内市販後症例の入力/入力データのQC業務1年以上（必須）を含む、PV業務3年以上の経験。

* ビジネスレベルの日本語能力。

* 英語の文書に抵抗感がないこと。

■■尚可

* データQCだけでなく、入力実務にも習熟していること。

* CIOMS 読解が可能な英語力。

* リモートワークに順応し、自発的にコミュニケーションをとれること。

■Responsibility

Perform QC checks on Data Entry of side effect information as a member of a post-marketing PV project.

■Workplace

Flexible Style Work (Home Based)

Commute to office (Shinagawa Seaside (Tokyo) / Shin-Osaka (Osaka) as needed.

■Requirements

■■Essential

* Over 3-year experience in PV case processing, including 1-year experience in Data Entry/ Data QC.

*Japanese language proficiency of business level.

* Being comfortable with handling documents in English.

■■Nice to have

* Proficiency in data QC but also in Data Entry practice.

* English proficiency enough to read and understand CIOMS.

* Being able to adapt to remote work and communicate voluntarily.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.