仕事概要
職種 | 専門職(コンサルタント、金融、不動産、専門サービス)/専門サービス(医療、福祉、教育、インストラクター) |
---|---|
業種 | 医療/ その他医療 |
雇用形態 | 未分類 |
ポジションレベル | その他 |
募集人数 | 1名 |
希望入社時期 | - |
必須語学力 |
日本語 (流暢に話せるレベル) 英語 (ビジネスレベル) |
活かせる語学 | - |
勤務時間 | その他 |
福利厚生・休暇 | |
ビザ取得支援 | - |
外国人従業員 | - |
仕事詳細
Company Overview
Manager, Technical Writing - Top Global Pharma Company
Job Description
Summary Of Key Responsibilities:
- Lead document writing assignments in conjunction with project team members for late stage programs in the preparation of content in support of regulatory submissions (eg, protocols, CSRs, Investigator’s Brochures, Briefing Documents, Orphan Drug Designation Dossier, JP-CTD for J-NDAs).
- Leads regulatory document writing and review processes for individual projects.
- Develops and maintains timelines for regulatory document generation, revision, and completion, in collaboration with other project team members and Regulatory Affairs/Operations.
- Coordinate and manage review cycles for documents in collaboration with subject matter experts, and lead discussions when needed.
- Edit/write clinical study report drafts from templates and interpret data as needed.
- Review and/or edit internal and external publications (eg, manuscripts, abstracts, poster presentations, white papers).
- Independently manage outsourced writing staff and projects.
Contribute to the development and maintenance of SOPs, templates, and style manuals.
- Provides communication and training on writing requirements and processes, templates, style guides, and SOPs within the department and cross-functionally, as required.
- Provides quality control (QC) review of various regulatory documents as needed.
- Independently solve problems, exercising sound judgment, appropriate interfacing, and flexibility within a dynamic environment.
Requirements
Qualifications:
- Bachelor's degree in Life Sciences with 4+ years’ experience in relevant field. Professional certification/credentials, experience with regulatory submissions is a plus
- In-depth knowledge of GLP, GCP, FDA regulations, ICH guidelines, and the drug development process.
- Successful track record of managing multiple projects in a fast-paced and deadline-driven environment.
- Impeccable attention to detail and excellent written and oral communication skills.
- Must be proficient in Microsoft® Suite (Word, Excel, PowerPoint, Visio). Experience with electronic document management and tracking systems a plus.
面接について
連絡先
Technical Writing Manager
RGFタレントソリューションズ株式会社
800 〜 1000 万円