CRA II
Hybrid · Osaka, Osaka, Japan or Tokyo, Tokyo, Japan
Job Summary
CRA II responsible for site qualification/initiation, monitoring (on-site or remote), and close-out activities with regulatory, ICH-GCP, and GPP compliance. Performs source data review/verification of CRFs, manages IP inventory and labeling per protocol, ensures ISF/TMF accuracy, supports subject recruitment/retention, and coordinates with sponsor teams. Requires strong communication, ability to adapt to changing priorities, and travel up to 75% for Real World Late Phase studies; role may involve global clinical monitoring activities and collaboration with sponsor affiliates and medical science liaisons.
Required Qualifications
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
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