Site Activation Specialist - Japan - Remote
Remote · Tokyo, Tokyo, Japan or JP
Job Summary
As a Site Activation Specialist, you will track study-specific site regulatory documents and follow up with sites or internal team members. Key responsibilities include supporting the development and review of informed consent forms, maintaining communication with sites for timely completion of start-up activities, collecting and reviewing essential documents, and supporting site identification activities including the negotiation of Confidential Disclosure Agreements. The ideal candidate will possess organizational and time management skills, have proficiency in MS Office applications, and an understanding of local healthcare systems. A background in medical or related science and at least one year of clinical research experience is required.
Required Qualifications
- A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy or other related science
- Minimum one year of experience in clinical research, preferably in site activation or regulatory-related function
- Previous experience within the pharmaceutical/CRO industry
- Good knowledge of ICH GCP, EU Clinical Trials Directive and other relevant clinical research conduct guidance
Desired Qualifications
- Multilingualism preferred; fluent in local language; working knowledge of English
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