Director, Ethics & Business Integrity Japan - About the job As Director, Ethics & Business Integrity within our Japan Compliance team, youll support the Head of E&BI in developing and maintaining effective compliance programs that uphold
Job Description 1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective
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
Job Purpose Provides leadership, oversight and manages the activities of within-country operational planning and delivery of Phase I-IV clinical trials in a specific country or cluster of countries; across all oncology areas (solid and blood) to
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports).
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.
CRA II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate
Job Summary ・Support the development, alignment and execution of Patients Value Plan(PVP) for B one Health Mission in Japan (BHM-J) ・Provides the strategic solutions and framework (such as segmentation and targeting) for Post Fracture Care to create
Primary Purpose / Regulatory Responsibilities: The primary purpose of a Project Manager (PM) is to ensure and elevate the level of country operations to realize patient value by transforming company’s strategy into project delivery in Japan. A
Department: GQP Compliance Group Report to: Head of Quality Japan General This role is to serve as an expert in the key quality management system for Japan subsidiary with regards to GxP requirements as well as
QA Expert This role is to serve as an expert in the key quality management system for Japan subsidiary with regards to GxP requirements as well as Japanese Pharmaceutical Laws. Support the Quality Manager with the
Responsibilities will include, but are not limited to, the following: 1. Lead JPN CAR-T commercial launch preparation 2. Leading the marketing for assigned brand / indication, developing annual operating plans and customer-based plans including financial forecasts
Duties: The Cell Therapy Scheduling and Logistics Specialist I will be responsible for scheduling and monitoring patient treatment schedules for the manufacturing of Celgene’s autologous cellular immunotherapy products. Responsibilities: • Coordinate with cell collection centers, cell therapy manufacturing
General Information Job Advert Title: Clinical Site Manager II（臨床開発モニター/ Site Monitor/ CRA） Location: Nihonbashi, Tokyo Division: Clinical Operations, Quantitative Sciences and China Development Employment Class: Permanent Description 【About Astellas】 Astellas is a global life sciences company
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
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
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce
Main Responsibilities and Accountabilities 1. Develop and strengthen capabilities across the Commercial organization Collaborate with relevant functions such as Sales, Marketing, Commercial Operations, and Medical to plan, implement, and improve training initiatives aimed at enhancing the
General Information Job Advert Title: Clinical Trial Manager Location: Tokyo, Nihonbashi Division: Early Development and Translational Science Employment Class: Permanent Description 【About Astellas】 Astellas is a global life sciences company committed to turning innovative science into
CRA I - Japan, Tokyo Hybrid: Office/Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility,