Johnson & Johnson キャリア

Janssen】R&D Japan, Documentation process expert

千代田区, 日本
Clinical Data Management


Requisition ID: 1805681495W

  1. 社内外のリソースの最適活用の判断
  2. スタッフのアサイン
  3. 進捗管理
  1. ベンダーへの業務委託
  2. 進捗管理
  3. 納品物の品質確認
  1. 他部門と協業した,高品質な文書作成プロセス構築
  2. AI,Robotic Process Automation(RPA)を活用した,新しい文書作成支援プロセス構築

Responsible for managing QC and translation operations of the drug development and application related documents to ensure optimal quality and efficiency by utilizing internal resources and vendors

[QC and Translation Management]
  1. Determine optimal use of internal and external resources
  2. Assign work to staff
  3. Manage Schedule
[Vendor Management]
  1. Coordinate external service providers
  2. Manage Schedule
  3. Confirm the quality of deliverables

[Process construction tasks]

  1. Build high-quality document creation processes with other divisions

Lead new process construction for document preparation by utilizing AI or Robotic Process Automation

・Medical Writing又はQCの経験がある方が望ましい
・基本的なPCスキル(Word,Excel,Power Point,etc.)
  1. Work experience in R&D of the pharmaceutical industry
  2. Medical writing or QC experience are desirable
[Skills and Capabilities]
  1. Basic PC skills (Word,Excel,Power Point,etc.)
  2. Excellent communication skills with writers and vendors
  3. Negotiation and coordination skills with writers and vendors
  4. TOEIC score: 700+
  1. No need
[Academic Requirement]
  1. Bachelor’s degree or higher
<Personal Skills>

Has an interest in innovative technology (ie, AI or RPA)

Be able to propose process improvements proactively

Be able to actively provide support to other departments

Janssen Pharmaceutical K.K. (7195)
Clinical Data Management
Requisition ID