募集要項
- 仕事内容
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Responsibilities:
Provide direct communication support and advice for key clinical documents CSR/IB/CTD clinical parts and/or regulatory defense for relevant clinical parts
Review additional clinical documents with the purpose of facilitating the translation of target product claims into a fully supported proposed product label, and to improve the communication quality of the documents
Lead the authoring of the clinical segments of briefing documents for PMDA consultations
Lead J-IB creation including communication with relevant global counterparts
Support the alliance of ADMIRe/MARS and other strategic alliances, as required, to help ensure the success of CSR production
Requirements:
Prior work experience in clinical drug development
Familiarity with GEL/ANGEL
Knowledge of drug development including key regulations (e.g., GCP, ICH, GLs)
Additionally, knowledge of drug development processes and guidelines
Knowledge of SOPs/WIs, particularly CSP/IC, CSR, IB, CTD
- 応募資格
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- 必須
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Prior work experience in clinical drug development
Familiarity with GEL/ANGEL
Knowledge of drug development including key regulations (e.g., GCP, ICH, GLs)
Additionally, knowledge of drug development
- 雇用形態
- Permanent
- 勤務地
- Osaka
- 年収・給与
- JPY6000000 - JPY9000000 per annum