Job summary
| Job category | Professional (Consulting / Finance / Real Estate / Professional Services)／Professional Services (Health Care / Welfare / Education / Instruction) |
|---|---|
| Industry | Health Care／ Pharmaceuticals |
| Employment type | Uncategorized |
| Position level | Other |
| Number of openings | 1 |
| Desired entry time | - |
| Required language skill |
Japanese （Fluent） English （Business） |
| Foreign language competence | - |
| Working hours | Others |
| Welfares / Leave systems | |
| Assistance in visa application | - |
| Number of foreign employees | - |
Work details
Company Overview
Biotechnology
Job Description
- Oversee the delivery to plan of studies performed by external partners (CROs, vendors and Site) and monitoring progress by identifying risk and solve operational issues.
- Lead and manage all activities related to site management and monitoring with agreed timelines, budget and company standard quality.
- Plan and deliver site selection/ patient recruitment strategy
- Ensure the quality of clinical study data by raising queries and deviation and resolve issues in a timely manner.
- Develop and manage risk mitigation plans and contingency plans to execute CRO/site management
Requirements
- University degree (or equivalent), preferably in medical or biological sciences or discipline associate with clinical research. Advance degree is preferred
- At least 6 years experiences from within the pharmaceutical industry or similar organization or academia experience
- Good experience of clinical development/drug development process in various phases of development and therapy areas
- Extensive knowledge of clinical operations, project management tools and processes
About interview
Liaison
Clinical Study Manager
RGF HR Agent
800 〜 1100 ten thousand JPY
