Basic purpose of the job Manage case processing activities for NBI’s investigational and marketed products including case submission to GPV and PMDA according to BI’s internal procedure and local regulation. Conduct safety risk management activities for
Be part of a top global pharmaceutical company in the industry. Take lead in CMC RA and QA activities as well as serving as the Hinseki. Client Details * Top global pharmaceutical company * Specializing in
Basic purpose of the job Manage case processing activities for NBI’s investigational and marketed products including case submission to GPV and PMDA according to BI’s internal procedure and local regulation. Conduct safety risk management activities for
At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview TE Connectivitys Sales & Marketing Support Teams assist with implementing
Job Purpose: The CPMS Asia/Japan Manager will provide technical therapeutic, and product development support for GlaxoSmithKline projects. Individuals will ensure the optimal application of Clinical Pharmacokinetic (PK), Pharmacodynamic (PD), and will have a proficiency in practice
This position involves applying a proven understanding of CMC elements and regulatory requirements to support, and provide guidance to Oncology/ Hematology teams in Japan. This position also supports all CMC regulatory filing activities including the preparation
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■ 職務内容 / Job Description Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in
