Description Kenvue is currently recruiting for: Legal Entity Controller - Japan/South East A sian Countries The Legal Entity Controller role primarily oversees the legal entit ies (LE) financial close process , financial reporting process, ensuring the
Description Kenvue is currently recruiting for: Legal Entity Controller - Japan/South East A sian Countries The Legal Entity Controller role primarily oversees the legal entit ies (LE) financial close process , financial reporting process, ensuring the
Do you have a strong background in non-clinical activities? We are looking for a Non-Clinical Expert to join our team at Novo Nordisk. If you are ready to contribute to the development, submission, and approval of new
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
We will use your ability to integrate/apply knowledge of global & Japanese regulations governing drug development to progressing Regenerons portfolio. This includes preclinical and clinical drug development programs, policies, and procedures. This is an exciting opportunity
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 of the
Career CategoryRegulatory Job Description Group Purpose Japan Regulatory Affairs provides leadership, expertise, and execution for the regulatory strategy to obtain and maintain clinical trial and marketing licenses for Amgen molecules in Japan in alignment with local business priorities
As a Manager in Market Access & Marketing, you will oversee insurance applications, regulatory submissions, and launch strategies for advanced cancer diagnostics. You will also lead a marketing team and drive commercial success for the Oncomine Dx Target
Take lead in RA activities to obtain product approval. Ensure effective submission requirements as well proper timelines of new/existing regulatory projects. Client Details * One of the top global pharmaceutical companies in the industry * Specializing in oncology,
Career Category Regulatory Job Description Job Summary Regulatory CMC Japan Manager is responsible for execution of the Japan-specific product strategies align with the global strategy. This position prepares and submits NDA/CTD/PCA/MCN/consultation dossiers in collaboration with Global Reg CMC
Take lead in RA activities to obtain product approval. Ensure effective submission requirements as well proper timelines of new/existing regulatory projects. Client Details * One of the top global pharmaceutical companies in the industry * Specializing in oncology,
Job Description SummaryContribute to the overall activities in drug development* toward obtaining the marketing authorization and maintenance activities of post marketing products in assigned TA area. * Drug development including development of drug, medical device, companion
About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
Role Summary The clinician medical monitor contributes towards providing medical and scientific expertise and oversight for Clinical Trials conducted worldwide with a primary focus in Japan and the Asia-Pacific region. The clinician medical monitor may be
About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
Job Description Summary-This is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific
Legal Entity Controller – Japan/South East Asian Countries-2407025143W Description Kenvue is currently recruiting for: Legal Entity Controller – Japan/South East Asian Countries The Legal Entity Controller role primarily oversees the legal entities (LE) financial close process,
Job Description SummaryThe SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies
Job title – Expert, Regulatory Affairs HNC Japan Location – Tokyo, Japan Job model – 2-year contract We are seeking a highly skilled and experienced Regulatory Affairs Specialist/Manager to manage the re-registration of pharmaceutical drug products in Japan.
