* この役割は、クリニカルメディカルマネージャーリードに報告します。 * 関連する治療分野内でKOL研究者、研究センターを特定・マッピングし、CDC（臨床開発センター）、地域、IO-SO、HQの臨床運営チームと緊密に協力して、フィージビリティおよび割り当てプロセスを実施します。 Client Details * ヨーロッパ製薬会社 Description * 価値のある医学的洞察を収集し、地域および地域のローカル／CDC内のチームに適切に伝達し、臨床試験実施のフィージビリティプロセスを最適化します。 * 関連する治療分野における専門知識を持つ専門家として、科学的コミュニティにおいてリーダーシップを発揮し、アドバイザリーボード、科学会議、ガイドライン、出版物を実施し、関連トピックに関してHCP（医療専門家）向けの地域協会と連携します * 臨床運営と協力して、フェーズI-IVの臨床試験の成功に貢献し、アドホックおよび計画訪問を実施し、研究者会議への出席を支援し、臨床試験へのKOLの参加を確保し、試験結果を伝えるために主要な研究者と連携し、地域レベルでの科学的保持および募集（SRR）活動に参加します。 Profile * 医学博士（MD）または医療分野のPh.D.を有し、強力な臨床および研究のバックグラウンドを持つことが望ましい。または、強力で関連するバックグラウンドを持つ薬剤師または理学修士でも可。 * 臨床または製薬業界で最低3年以上の経験があり、大学または製薬業界での人間医療研究の確固たる経験が必要。 * 関連する治療分野の専門家であり、査読付きジャーナルでの著者経験があることが望ましい。臨床試験の主研究者または副研究者としての経験があると尚良い。 Job Offer * 全国の患者さん、さらに海外の患者さんに幅広い影響を与える * グローバル大手企業での有意義なポジション * 安定したキャリアパス、海外経験の機会、魅力的な給与 Page Group Japan is acting as
Craft engaging social media content tailored to Japanese audiences and manage social media presence for a leading financial infrastructure platform in Tokyo under a Global B2B Marketing Agency. Client Details Join a pioneering company at the forefront
Be part of a critical member in the RA organization. Lead in RA development/strategy activities to obtain product approval for various unmet medical needs. Client Details * Global leading pharmaceutical business specialising in womens health * With
職種 正社員 職務明細 HirePlanner.com is a growing HR Tech Start-Up in Japan. We are looking for a motivated sales manager to help us grow our presence in Japan and prepare to scale internationally. Our technology and
職種 正社員 職務明細 HirePlanner.com is a growing HR Tech Start-Up in Japan. We are looking for a motivated sales representative to help us grow our presence in Japan and prepare to scale internationally. Our technology and
職種 フルタイム(契約) 職務明細 We are seeking a dynamic and driven individual to join our marketing agency as a business development lead with a focus on marketing. In this role, you will be responsible for driving new business growth
* Lead and manage a team of biostatisticians and data managers to ensure the delivery of high-quality and timely statistical analysis plans, data management plans, and data analyses for clinical trials. Client Details * Our client
* Lead and project management of the following studies: - CSS (Company-led research) - IIS (Doctor-led research) - Collaborative study - Including oversight of external CRO Client Details * Leading global CRO business, with rich project
* The Safety Management Officer will oversee all safety management and pharmacovigilance (PV) activities in Japan. * This role involves ensuring compliance with local regulations, managing risk, and maintaining high standards of safety for all products.
* As a registered safety management supervisor required by Japan GVP, oversee and ensure overall safety related tasks for marketed products 企業情報 * Global Biotech company * Great pipeline with steady business status 職務内容 * Ensure
Responsible for the development and analysis of contractual relationships. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. 企業情報 * Mega US pharmaceutical * Wide range of pipelines including
Program ownership in Japan with final accountability for clear definitions of program goals, plans, decisions and deliverables to meet those goals. Ready to level up to be a leader of Global Clinical Project Management? 企業情報 *
As a clinical trial manager, you oversee the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements while collaborating closely with cross-functional teams to drive successful trial completion and contribute
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
This role entails aiding in the execution of clinical trials in new therapy areas, offering medical insights from engagements with key opinion leaders and professional associations, while reporting to a lead within the team overseeing these
* Develop and monitor annual business plans and objectives, providing updates and resolving issues in collaboration with senior management and stakeholders and Japan GM. * Execute business plans, coordinating review meetings and managing cross-functional projects while
* 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
Take lead in medical writing activities in authoring clinical/regulatory documents as well as submission requirements to obtain product approval. Align with global business strategies for local requirements Client Details * One of the top global biopharmaceutical
電動自転車と電動スクーターを使用した交通を専門とするMaaS企業。 Japanese MaaS company specializing in transportation using e-bikes and e-scooters. 何をしますか？ * 会社からの戦略やアイデアに基づいたブランドアクションを開発します * タイムラインと責任者に対するリソースの割り当てなど、プロジェクトに必要な要件を含むアクションプランを作成します * 外部企業とのパートナー交渉 * ブランドのPRとプロモーション What will you do? * Develop brand actions based on strategies and ideas from the company
Leverage your fluency in Japanese and business-level English to develop and manage high-quality proposals for global clinical research projects. Contribute to groundbreaking medical advancements in a dynamic, collaborative environment while enjoying competitive compensation and professional growth
