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Good Clinical Practiceの求人-武蔵野 - 21 Job Positions Available

1 – 15 of 21 jobs
Regeneron jobs

Are you ready to make a meaningful impact on clinical development programs in Japan? At Regeneron, we are seeking a dedicated Medical Director, Clinical Sciences, to join our dynamic team. In this pivotal role, you will collaborate closely

Regeneron  28 days ago
Astellas Pharma jobs

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 committed to

Astellas Pharma  21 days ago
Eucalyptus jobs

About Eucalyptus We’re on a mission to make good health last a lifetime. More than 1 billion people live with obesity worldwide, driving preventable chronic conditions. We’re here to build better long-term care. Euc is the company

Eucalyptus  16 days ago
Randstad Sourceright - Japan jobs

The GCDSE provides clinical and R&D expertise, guidance and direction in the context of the region/country, in which they operate. As the leader of the Clinical (or Extended Clinical) Team, the GCDSE is the clinical representative in global project teams

Randstad Sourceright - Japan  1 day ago
Pfizer jobs

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 (GCP), and Pfizer

Pfizer  28 days ago
Fortrea jobs

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). Manage and

Fortrea  24 days ago
Syneos Health jobs

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

Syneos Health  22 days ago
Randstad Sourceright - Japan jobs

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients. Acts as a field-based expert, building relationships with External Experts as trusted scientific partners.

Randstad Sourceright - Japan  22 days ago
Randstad Sourceright - Japan jobs

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients. Acts as an office-based scientific expert, collaborating with internal and external stakeholders. Translates scientific

Randstad Sourceright - Japan  22 days ago
Randstad Sourceright - Japan jobs

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

Randstad Sourceright - Japan  22 days ago
Randstad Sourceright - Japan jobs

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

Randstad Sourceright - Japan  22 days ago
Flatiron Health jobs

Were looking for a Manager, Strategic Partnerships & Communications, Japan to help us accomplish our mission to improve and extend lives by learning from the experience of every person with cancer. Are you ready to be

Flatiron Health  13 days ago
MSD jobs

Job Description 【職務内容】 治験責任医師候補及び治験実施医療機関候補の調査 治験の依頼及び契約 各治験施設での組み入れプランに沿った組み入れ依頼及び組入れ状況の確認 治験施設での有害事象情報の収集及び安全性情報の治験施設への伝達 必須文書の作成及び授受 モニタリング報告書の作成 症例報告書のカルテとの照合 治験の終了手続き 開発品及び競合品の情報収集 【必要とする資質】 医師、CRC等に対するコミュニケ-ション能力 社内プロジェクトメンバーの一員として自発的に行動できる積極性及び協調性 治験薬概要、治験実施計画書等を理解し説明できるプレゼンテーション能力 医学関連全般の基礎知識 グローバル研究開発本部の他部門と協調しながら業務を遂行できる能力 パワーポイント、ワード、エクセルのコンピュータースキル 英語力(TOEIC 730以上:メールでのビジネスが可能なレベル) 【望ましい資質】 GCP、社内SOPの知識(異動後に研修あり) 担当する治験薬、疾患領域に関する知識(異動後に研修あり) 英会話能力(プレゼンテーション、テレカンファレンスなど) ジェネラルメディスン・感染症ワクチン関連の専門知識 Required Skills: Clinical Data Management, Clinical Trials Monitoring, Drug Development, English Language,

MSD  10 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Warehouse, Will work with hazardous/toxic materials Job Description As part of the Thermo Fisher Scientific team, you’ll discover

Thermo Fisher Scientific  8 days ago
Johnson & Johnson jobs

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 our

Johnson & Johnson  22 hours ago

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