
RWE Specialist
Tokyo, Japan Permanent Posted on Mar. 26, 2025 Closing on Apr. 25, 2025RWE Generation Partnering募集要項
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Job title: RWE Specialist
Location: Japan, Tokyo
Approximately 40% Remote work
Job type: Permanent
About the Job
Our team
開発品、製品におけるメディカルニーズ、Data Gapを踏まえたClinical Question/ Research questionをメディカルマネジャーと検討し、科学的に適切な研究デザインの立案、データソースの選定、解析の計画と実施、論文化を含む研究結果の報告を専門家として支援医薬品リスク管理計画書の安全性検討事項に基づくClinical Question/ Research questionに対し、社内外の専門家とのコミュニケーションをリードし、科学的に適切な研究デザインの立案、データソースの選定、解析の計画と実施、報告書の作成を専門家として支援外部データサイエンティストとのネットワークを構築し、高い専門性を生かしてリアルワールドエビデンスの創出を推進日本の医療情報データベースに関する情報集積及び社内に存在する医療情報データベースの一元管理を行うと共に、医療情報データベースへのアクセスツールを用いた社内ステークホルダーへのRWD情報の提供
Our team
Discuss clinical questions/ research questions with the medical manager based on the medical needs and the data gap of the products, and support the development of scientifically appropriate research design, selection of data sources, planning and implementation of analysis, and Publication as an expert.Lead communication with external epidemiologists such as PMDA in response to clinical questions/ research questions based on safety considerations in the drug risk management plan, and development appropriate study designs, select data sources, and create and implement analysis plans.Build a network with external data scientists and promote the creation of real-world evidence by leveraging your high level of expertiseCollect information on Japan's medical information database and centrally manage the medical information database existing within the company and provide RWD information to internal stakeholders using a tool to access the medical information database.
About you
Experience, Education, Soft skills and Languages
治験または観察研究等における薬剤疫学、生物統計に関する十分な知識、5年以上の実務経験
データサイエンスやリアルワールドデータを含む医療情報データに関する十分な知識
SAS、R、Python、SQLなどのプログラミング言語の知識と5年以上の実務経験薬機法やGPSPに関する基知識又はGxP領域での業務経験
医薬品や疾患に関する医学的、科学的な知識と思考
プロジェクトマネジメント、業務管理能力
ステークホルダーとの調整やコミュニケーション能力、リーダーシップ
英語でのコミュニケーション能力
変化に向けて自ら行動する強い行動力と新たな手法などにチャレンジする好奇心
Deep knowledge of pharmacoepidemiology and biostatistics in clinical trials or observational studies, DB study etc., and at least 5 years of work experience
Knowledge of data science and technology related to healthcare data
Knowledge of programming languages such as SAS, R, Python, SQL, etc. and at least 5 years of work experience
Knowledge of Pharmaceutical law and GPSP requirements and/or experience of GxP related activities
Medical and scientific knowledge and thinking about pharmaceuticals and diseases
Project management/task management ability
Coordination and communication skills with stakeholders, leadership
Communication ability in English
Strong ability to take action for change and curiosity to take on new challenges
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