R&d Oncology Clinical Science Clinical Research Sr. Scientist

Merck Merck · Pharma · Tokyo, Japan

This role at Merck focuses on clinical research in oncology, involving the planning, execution, and reporting of clinical trials. The scientist will collaborate with internal and external stakeholders, including regulatory bodies, to support the global development of new oncology drugs. Responsibilities include inputting into development strategy, preparing regulatory submission documents, managing clinical trial protocols, monitoring data, and contributing to publications.

What you'd actually do

  1. 開発戦略策定の補佐 (早期及び後期開発計画書への日本の臨床試験計画のインプット)
  2. 開発戦略に基づいた機構相談の立案や資料作成のサポート、及び照会事項に対する回答作成
  3. 治験実施計画書の立案及び翻訳・作成
  4. 治験総括報告書及び承認申請資料(CTD)臨床パートの作成 (メディカルライターと協働)及びレビュー
  5. 承認申請後の照会事項に対する回答作成、適合性調査対応

Skills

Required

  • Clinical Sciences
  • Communication
  • English Language
  • ICH GCP Guidelines
  • Protocol Development
  • Translations

Nice to have

  • Clinical Study Design
  • Clinical Study Management
  • Clinical Study Reports
  • Clinical Trial Planning
  • Informed Consent
  • Oncology
  • Oncology Trials
  • Strategy Plan

What the JD emphasized

  • 医薬品臨床開発業務の経験
  • 治験実施計画書の作成経験
  • 社内(国内・外)関連部門及び外部専門医との密接な協働作業のためのコミュニケーションスキル
  • 英語力(TOEICスコア730点以上目安)