* Stepping-stone from Clinical Research Associate to Project Management * Support and collaborate with Project Management team and global clients and gain valuable on the job training Client Details * Global Healthcare business that partners with
Oversee safety and pharmacovigilance in clinical trials, including adverse event analysis, reconciliation, safety reporting, regulatory compliance, stakeholder liaison, and document management. Client Details Leading pharmaceutical innovator driving the forefront of medical discovery through cutting-edge research and development
Responsible for generating post-marketing safety evidence of products using real-world data in Japan. 企業情報 * Top Global Pharmaceutical Company * Highly specialized in Oncology area with rich pipeline 職務内容 - Creates study report, and Re-examination dossier
Leading the local trial team to deliver results compliant with assigned protocols, codes of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements. Actively contributing to process improvement and site management, you will train and
Controller position to support the CFO at a prestigious luxury brand | Career path, WFH available, Central Tokyo Client Details Our client is a world-renowned luxury accessories brand known for its exquisite designs, craftsmanship, and use
Lead in RA activities to obtain regulatory approval for company products. Expand the business into the Japanese market. Client Details * Global medical device company operating in 40 countries around the globe * Specializing in up to
Take lead in QC for quality tests and designs. Ensure proper documents and regulatory requirements are correct. Client Details * One of the leading global pharmaceutical companies in the industry * Specializing in Immunology, Neurology, and rare
Lead in RA activities to obtain regulatory approval for company products. Expand the business into the Japanese market. Client Details * Global cosmetic medical device company * Specializing laser treatment for skin treatment * year on year
* At the front line of communication with stakeholders at hospital sites / clinics, youll manage clinical aspects of full-service global trial projects. Your responsibilities will include ensuring timelines, targets, and standards are met for clinical
* Responsible for preparation and submission of expedited and periodic safety reports to Regulatory Authorities, Ethics Committees and Investigators, adhering to all data privacy guidelines, Good Clinical Practices (GCPs), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program-specific
* This position will be responsible for managing assigned clinical studies globally and locally, overseeing study activities, budgets, timelines, and vendor relationships. * The role involves leading a multifunctional team, ensuring adherence to regulatory requirements, managing study
* Responsible for supporting the Project Management group to ensure smooth and effective study delivery through organising of important documents and files. Client Details * European headquartered, pharmaceutical company with a mission to help patients with
As an IT support, you will work with a small team of IT engineers and will ensure smooth support of day to day technical operations of trading floor which will be the core component of your
* Financial control under IFRS and JGAAP * Statutory reporting to Head Office * Timely and accurate review of securities and bank regulatory reports, liaison with regulators * Management reporting and group performance analysis Client Details Our
A Clinical Scientist at this renowned biopharmaceutical company contributes to cutting-edge research, particularly in oncology, driving advancements in patient care. They play a pivotal role in conducting clinical trials, analyzing data, and contributing to the development
This is Implementation Consultant/Project Management Position for American software company that develops cloud-based solutions to automate enterprise financial and accounting process. Client Details This is an US-based leading provider of cloud software that automates and controls
職種 正社員 職務明細 Tokyo-based Langley Esquire is a public affairs consulting firm specializing in government relations, strategic communications, and public policy. We overcome challenges at the nexus of government, industry, and society. With over 30 years
職種 正社員 職務明細 This is a role directly hired by Mazars in Singapore, and will be based in Singapore. The Manager manages a portfolio of engagements to deliver high-quality audit services. You will provide leadership on
職種 正社員 職務明細 A generalist player in establishing the overall business operations for Spenmo’s release in Japan, mainly in customer support and digital marketing スキル・資格 ・Minimum 1 years of relevant Fintech/ B2B software product marketing, sales
職種 正社員 職務明細 LVMH Group is a world leader in luxury with a diverse portfolio of Maisons known for the exceptional creativity, craftsmanship and heritage. We are committed to delivering unparalleled experiences to our customers while
