[JDSU] 医薬品安全性統括部 ケースマネジメントチーム(一般社員) (Staff, Case Management, Japan Drug Safety Unit)

Pfizer · Tokyo

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1.主な職務における成果責任/ Description of Primary Role & Responsibility
A. 市販製品・治験薬の安全性情報(有害事象)収集、評価 / Collection and Assessment of safety information (adverse event information) of marketed/investigation Pfizer products
B. グローバル安全性データベースへのデータ入力と管理 / Data entry and management on Global Safety Database
C. 日米欧の法規制の遵守、安全性コンプライアンス維持 / Compliance with laws and regulations of Japan, the United States and Europe, and maintenance of safety compliance
D. 国内、海外の社内及び規制当局の査察・監査対応 / Contribution to domestic and foreign internal audit/regulatory inspection
E. 個別安全性情報における照会事項対応 / Response to regulatory query regarding to Individual Case Safety Report
F. グローバル安全性業務プロセスの構築に係るプロジェクトへの参画 / Contribution to projects relating to development of process relating to global safety

2.応募資格/ Qualifications
【スキル要件 / Skill requirements】

【職務経験 / Background requirement】
• 日本語能力(日本語で日本の規制を理解し、説明することができる。規制当局向けの文書を日本語で作成することができる。) / Fluent Japanese language capability (able to understand and explain Japanese regulation in

Japanese, able to develop regulatory documents to be submitted in Japanese.)


【勤務地 / Location】
東京本社 / Tokyo Headquarter


※応募時は、日本語・英語両方の応募資料の提出をお願いします。 / Please submit application form in both Japanese and English.

  
Work Location Assignment: Hybrid

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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Medical

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