* Responsible for the following Case processing tasks as a member of the clinical information or post-marketing drug or medical device safety information management project: - Receipt of information on adverse events, entry in database - Creation
* Lead activities in global clinical trials, ensuring the successful planning, execution, and oversight of site monitoring activities. * Provide mentorship to less experienced staff, and foster a learning culture within the Clinical Development & Operations team, promoting
* Join our client as a Senior Associate Clinical Contracts & Budgets, where youll lead end-to-end contracting processes for clinical studies, ensuring seamless operations and payment accuracy. Fluency in Japanese is essential, along with a knack for negotiation, attention
Join our global client organization as the Senior Manager or Associate Director of Biostatistics, where youll leverage your statistical expertise to lead and support clinical trials in Japan. Utilize your fluency in Japanese and business-level English to collaborate