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
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
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.
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.
Job Description SummaryAccountable for the oversight and coordination of program and study level (re-)feasibility assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes, GCP, ICH and regulatory requirements. This
Job TitleRegulatory Affairs Senior Manager - Japan Job Description Regulatory Affairs Senior Manager Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through
