Description Kenvue is currently recruiting a PR Specialist. This position reports into Senior Manager, External Communications, and is based in Tokyo, Japan. Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built
Overview: This position is accountable for leading in the development of clinical evidence generation and dissemination strategies across assigned projects. Main responsibilities and duties: • Lead to evidence generation strategy with collaboration relationships with all cross-functional
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
Description Kenvue is currently recruiting for: Communications Manager - Japan This position reports to Head of Corporate Affairs Japan and is based at Tokyo. Who we are At Kenvue , we realize the extraordinary power of
職務の目的および主な業務内容 Job Purpose & Key Responsibilities Job Purpose & Key Responsibilities Provides medical and scientific support to the Therapeutic Area (TA) Business Units of Rx, most notably, sales and marketing. Ensures that all company scientific, promotional
We are seeking CRM Tech Lead for Japan Commercial and Medical who will contribute to the success of our Japanese business by leveraging global strategies while focusing on the unique needs of the local market. This
Manage overall accounting functions, including accounts payable, expense reports, treasury, inter company transactions, inventory, and fixed assets, while ensuring accurate SAP entry for vendor invoices and processing Concur expense reports. Additionally, prepare financial statements, assist with
* Conduct comprehensive quality assessments on all research reports produced to ensure accuracy, clarity, and adherence to established standards * Analyse research reports for factual correctness * Verify data integrity, methodology consistency, and adherence to regulatory and
* 目標配分割合変更時等発生時の法定/非法定書面の更新、提出対応 * ファンド関連書類(目論見書、約款、商品概要等)の準備対応 * フラッシュレポートの作成、テンプレートの管理対応 * 月次書類や運用報告書のスケジューリング * 新規ファンド設定、繰上げ償還、約款変更、販売会社追加対応 Client Details Global asset management firm Description * 目標配分割合変更時等発生時の法定/非法定書面の更新、提出対応 * ファンド関連書類(目論見書、約款、商品概要等)の準備対応 * フラッシュレポートの作成、テンプレートの管理対応 * 月次書類や運用報告書のスケジューリング * 新規ファンド設定、繰上げ償還、約款変更、販売会社追加対応 Profile * 5-15 years of regulatory filing and prospectus changes
As a Senior Data Manager, you will lead a team to ensure high-quality data management in clinical trials, driving regulatory compliance and project success. This role offers impactful work and career advancement in a leading organization focused
The Japan Safety Pharmacovigilance Associate ensures compliance with local safety regulations and executes pharmacovigilance processes. The role involves collaborating with cross-functional teams and regulatory authorities to manage safety data effectively. Client Details The client is a leading
Be part of one of the leading biopharmaceutical companies in the industry. Take lead in RA development strategies as well as lead the RA team. Client Details * Be part of one of the top global
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
Be part of a top global biopharma start-up recently entering the Japanese market. Take lead in RA strategy/development to obtain and maintain product approval. Client Details * One of the top global biopharmaceutical companies specializing in
Be part of one of the top global pharmaceutical businesses in the industry. Take lead in GCP audits for the company to ensure regulatory compliance. Client Details * One of the top global pharmaceutical companies in the
Be part of one of the top global biopharma business in the industry. Take lead in QA activities for the business to ensure effective compliance. Client Details * Be part of one of the top global
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
JOB DESCRIPTION: 職務記述書 募集用 RA Senior Specialist, Grade 14~15 体外診断用医薬品及び医療機器の新規申請品目の薬事申請、保険適用に関する戦略を関連部門と協議の上策定する。 担当事業部製品に対し、MKTG、R/Dと薬事申請、保険適用のプランを部門長と共に行う。 プランに従い、新規製品の薬事申請、保険適用及び必要な社内の手続きを行う。 製品の変更連絡を評価し、返答を実施する。該当する場合、必要な薬事上の手続きを行う。 広告、顧客レター等のタイムリーなレビューを行う。 薬事部メンバー及び他のプロジェクトチームメンバー等に薬事申請、薬事規制、法規制等についてトレーニング を行う。 業界団体(臨薬協、AMDD等)の活動に参加し、当社のコンプライアンスポジションを優位な状態に維持すると 共に、業界の発展に寄与する。 担当事業部関連業務の進捗状況を上長へ報告する。申請戦略やコンプライアンス戦略、その他薬事上の決定でリーダーシップを取る責任がある。 厚生労働省、PMDA、都道府県庁及び他社と薬事上の問題についての解決案を策定し、上長に適切な進言し、また必要に応じて直接交渉を行う責任がある。 薬事規制とビジネスとのバランスを取りつつ、コンプライアンスを遵守する方策を考え、上長へ進言をする。その他、上長より指示された業務を遂行する。 TOEIC:600点以上 海外製造所との電話会議の実施が必要。 •Develop strategies for new IVD applications and reimbursement coverage. •Conduct IVD submission applications,
Export Control & Government Affairs Manager Japan Introduction to the job ASML brings together the most creative minds in science and technology to develop lithography machines that are key to producing faster, cheaper, more energy-efficient microchips.
Product Manager – Quantile (Post Trade Solutions) Quantile brings a proven, unique blend of business, quantitative and technology skills to the industry, to provide post-trade risk reduction services to major derivative market participants. Our focus is