Manager, Global Clinical Site Management Location: Japan HQ/Tokyo, Nakano About the role: Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Job title: PMS Planning and Management Specialist • Location: Tokyo, Japan - About the job As a PMS Planning and Management Specialist within our Regulatory Affairs team, youll help ensure the safety and integrity of new medicines by
Job Title: PMS Planning and Management Head • Location: Tokyo, Japan - About the Job As PMS Planning and Management Head within our Regulatory Affairs & Patient Safety team, youll lead a high-performing group responsible for shaping post-marketing
Job Description 医薬品開発プロジェクトにおけるプロジェクトマネジメントおよびアライアンスマネジメント業務 – プロジェクトマネジメントおよびアライアンスマネジメントのスキルや専門知識、一般的ビジネススキル、および疾患領域特異的な知識や経験を基に、部門横断的および戦略的視点からプロジェクトを推進する。 ・プロジェクトスコープの特定と開発戦略の立案を推進する。 ・開発戦略の実行状況やタイムライン等の進捗管理を行う。 ・リスクマネジメント、ステークホルダーマネジメントを遂行する。 ・ガバナンスとプロジェクトの接点となり、開発戦略の意思決定を推進する。 ・US本社プロジェクトマネージャーやチームメンバーと協働し、世界同時開発を推進する。 ・他社との協働にあたり、アライアンスマネジメントを遂行する ・特許等様々な観点から、製品の価値最大化に貢献する。 【必要なスキル・経験】 ・5年以上の製薬会社での勤務経験 ・3年以上のプロジェクトマネジメント（もしくはそれに相当する）経験 ・ビジネスレベルでの英語力 【尚可要件】 PMP (Project Management Professional) 資格 知的財産関連資格および実務経験 ※ Grade：P3 (Sr. Specialist)での募集ですが、ご経歴によりP2 (Specialist) やP4 (Associate Director)で採用する場合がございます。 Required Skills: Adaptability, Adaptability, Business Functions,
Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of
Legal Solutions Consultant Are you keen to combine your legal industry knowledge with cutting-edge technology? Our Legal Solutions Consultant is responsible for driving gross sales by proactively developing and helping to close solution sales opportunities. By
Japan Study Managerは、日本国内において治験の管理・監督を担い、CROや治験実施医療機関と連携しながら、治験参加者の安全と福祉、治験の品質を確保し、治験の計画通りの実施をリードします。グローバル・ローカル双方と連携し、課題解決や進捗管理も担当します。 JOB SUMMARY & RESPONSIBILITIES Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices
Job Overview: Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement. Summary of Responsibilities: Accountable for the overall payment management of assigned
Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on
About the Team / Department You will join a global Project Management team supporting Linguistic Validation (LV) and eCOA projects for clinical trials. The team works closely with internal stakeholders, clients, and external vendors to deliver high-quality, compliant,
Type de contrat : CDI Temps de travail : Temps plein Lieu: Shinjuku City Salaire: 500000 JPY (¥) - 650000 JPY (¥) / mois Japan Experience Since 1981, weve been a leading tourism company, specializing in
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 title: Clinical Operations Study Country Lead (COSCL) Location: Tokyo, Japan About the job Our Team: We are seeking a highly motivated and experienced Clinical Operations Study Country Lead to support local clinical trial operations. The COSCL
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
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.
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.
MAIN RESPONSIBILITIES / DUTIES JOB POSITION PURPOSE • Act as the Amyloidosis team lead and line manager, leading a team of MAS. Shape the local strategy and ensure the delivery of scientific‑medical expertise and exchange with