Leading the local trial team to deliver results compliant with assigned protocols, codes of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements.
Actively contributing to process improvement and site management, you will train and mentor Site Managers (SMs) and other Local Trial Managers (LTMs).
Client Details
One of the leading pharmaceutical companies globally recognised especially in the field of oncology.
Description
* Assess country and site suitability for trials, considering feasibility and do-ability.
* Lead local trial planning activities, including SOP development, budget management, and risk assessment.
* Serve as a local expert on protocols and regulatory affairs, while maintaining relationships with stakeholders.
Profile
- BA/BS degree required, preferably in a health or science-related field
- Solid understanding of the drug development process
- Proficiency in both Japanese and English
Job Offer
Involvement in cutting-edge drug development for the global market.
Page Group Japan is acting as an Employment Agency in relation to this vacancy.

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