- 東京23区正社員1300万円 - 1500万円外資系企業
- Responsible for design and execution of clinical trials within the haematology cell therapy business
- Lead clinical trials at a country level
Work for industry leading oncology focused biopharmaceutical company
Contribute to development of innovative new cell therapies
求人を保存 求人を見る - 日本正社員外資系企業
- Data management activities across broad range of global clinical trials
- Work closely with US Office and sponsors to ensure effective and timely execution of project deliverables
Work in Multinational Environment
Contribute to Global Clinical Trials
求人を保存 求人を見る - 日本正社員外資系企業
- The GCP Auditor will be a critical team member who contributes to the implementation of a risk-based GCP audit program and provides oversight / management of the GCP consulting program.
- Promote continual improvement regarding customer satisfaction with emphasis on GCP consulting services.
Work in a World-winning Global CRO
Lead GCP Consulting Program to Global Healthcare Clients
求人を保存 求人を見る - 東京都正社員600万円 - 900万円外資系企業
You will support the management of investigative sites and ensure that all sites adhere to the requirements and regulations governing Clinical Research. You will support feasibility, study start-up, assisting sites during maintenance and closing out sites.
Join a growing top-5 CRO
Comprehensive training and development
求人を保存 求人を見る - 東京都正社員1700万円 - 2200万円外資系企業
Working as the leader of a cross-functional study team and for a mix of sponsors. The Project Director is responsible for owning and achieving interim and final contractual deliverables for assigned projects/programs, according to the time, quality/scope and cost constraints.
Join a growing top-5 CRO
Lead a cross-functional study team
求人を保存 求人を見る - 日本正社員外資系企業
- Responsible for conducting oversight of each project and/or trial level
- Responsible for guaranteeing the high quality of a trial, identifying potential issues and contributing to root cause analysis and CAPA
Responsible for Oversight of Clinical Operation Excellence
Contribute to Approval of Innovative New Medicines at Leading Pharma Company
求人を保存 求人を見る - 東京都正社員500万円 - 900万円外資系企業
CTDライティングの作成.
プロジェクトチームのメディカルライティングにおける管理.
メディカルライティングにおいて強いキャリアパス
インターナショナルなノウハウを身につけ、グローバルなコミュニケーションを体験する機会
求人を保存 求人を見る - 日本正社員外資系企業
Collaborate with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review.
Design and implement clinical protocols and data collection systems.
Utilize Data Management Expertise to Expedite Clinical Trials
Contribute to Approval of Innovative Medicines
求人を保存 求人を見る - 日本正社員外資系企業
- Prepares, conducts Quality Assurance audits, generates audit reports, communicates results to the relevant QA management and external relevant stakeholders (e.g., Clinical Operations), and interacts with various teams to ensure corrective and preventative actions are taken
- Responsible for guaranteeing quality and compliance of trials, identifying issues and leading root cause analysis and CAPA
Responsible for Oversight of R&D Quality and Compliance
Contribute to Approval of Innovative New Medicines for Growing Biopharma Company
求人を保存 求人を見る - 東京都正社員外資系企業
- Responsible for management of Clinical Quality oversight of each project and/or trial level to ensure adherence to Quality & Compliance guidelines
- Responsible for guaranteeing the quality and compliance of a trial, identifying potential issues and contributing to root cause analysis and CAPA
Responsible for Conducting Oversight to Ensure Quality Compliance
Contribute to Approval of Innovative New Medicines
求人を保存 求人を見る - 東京23区正社員日系企業
診療放射線技師資格保有者を求めています。
先行他社がいる業界ではなく、自らが進む道を切り開いていく面白さがあります。診療放射線技師資格保有者を求めています。
先行他社がいる業界ではなく、自らが進む道を切り開いていく面白さがあります。
求人を保存 求人を見る - 日本正社員外資系企業
- Lead data management operations across broad range of global clinical trials
- Act as project leader and functional lead as well as primary contact for sponsors
Utilize Data Management Expertise to Expedite Clinical Trials
Contribute to Approval of Innovative Medicines
求人を保存 求人を見る - 日本正社員外資系企業
- Lead data management operations within Japan for global clinical trials
- Facilitate smooth operation of EDC activities for internal and external stakeholders
Utilize Data Management Expertise to Expedite Clinical Trials
Contribute to Approval of Innovative Medicines
求人を保存 求人を見る - 日本正社員外資系企業
- Produce an manage SAS are met within the allocate timeline
Utilize Statistical Programming Expertise to Expedite Clinical Trials
Contribute to Approval of Innovative Medicines
求人を保存 求人を見る 
日本正社員外資系企業- Responsible for leading the following safety management tasks as a manager of the clinical and post-marketing safety:
- Receipt of information on adverse events, entry in database
- Creation of case description (Japanese, English)
- Primary evaluation of the necessity of reporting a defect to PMDA
- Creation of adverse drug report
- QC check
Develop Innovative New Drugs at a Leading Global Contract Research Organization
Contribute the Safety and Wellness of Patients Globally
求人を保存 求人を見る- Responsible for leading the following safety management tasks as a manager of the clinical and post-marketing safety:
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