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- Clinical trial management
- Top gaishike pharmaceutical manufacturer
About Our Client
Our client is a major U.S. pharmaceutical manufacturer looking for skilled employees in their Japan office
*Work closely with monitors, internal stake holders, trial associates, contract administrators and clinical quality managers to provide up to date and accurate site reports for use by the internal clinical department.
*Organize trial scheduling and relay the appropriate information to the team members making sure that the timeline outlined in the protocol is being followed in an appropriate manner.
*Select facilities and manage the budget of the trial, preparing CAPAs for use by the facility auditors.
*Work with outsourcing companies to achieve timeline-related requirements.
The Successful Applicant
*Familiar with ICH-GCP guidelines and protocols related to site management
*Experience of managing more than one clinical trial (preferable global)
*Strong leadership skills and ability to be a role model for following compliance issues.
*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