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Senior Site Clinical Monitor
- Clinical development
- Top gaishike pharmaceutical manufacturer
About Our Client
Our client is a major U.S. pharmaceutical manufacturer looking for skilled employees in their Japan office
*Monitors activities conducted by clinical investigative sites as they relate to clinical studies to ensure successful execution of the protocol.
*Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations - GCP, ICH guidelines and SOPs
*Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
The Successful Applicant
*BSc or higher in a bioscience related field OR related professional qualification
*3+ years of experience in clinical development, ideally monitoring
*Familiar with regulations governing clinical research.
*Fluent Japanese, Business-level English
*Experience working for a pharmaceutical manufacturer
What's on Offer
*8M - 12M JPY salary depending on experience
*Financial and other bonuses and perks