About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better
Title:Special Operations Case Manager (Okinawa,Japan)) THIS POSITION OFFERS RELOCATION. Belong. Connect. Grow. with KBR! KBR is a company of innovators, thinkers, creators, explorers, volunteers, and dreamers; but we all share one goal: to improve the world responsibly and
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. PSI is a leading Contract Research Organization with more
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
Basic Purpose of Job Manage case processing activities for Nippon Boehringer Ingelheim’s investigational and marketed products including case submission to Global Patient Safety and Pharmacovigilance (PSPV) and PMDA according to Boehringer Ingelheim (BI)’s internal procedure and
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice, Warehouse Job Description Essential Duties and Responsibilities Understand key business drivers and leverage knowledge of the regulatory framework and environment in Japan to propose regulatory solutions that enable the delivery of
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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
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
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000
職務内容 スタディ・マネジャーは、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
臨床試験の運営をリードするポジションとして、グローバルチームや外部パートナーと連携しながらプロジェクトを推進します。試験の進行管理・品質確保・リスク対応まで幅広く担当する役割です。 企業情報 グローバルに事業を展開する医薬品関連企業で、臨床開発および医療ソリューションに関する事業を行っています。複数の専門領域のメンバーが在籍しており、各種プロジェクトにおいて協働しながら業務を進める体制です。 職務内容 * 臨床試験（初期〜後期フェーズ）の運営および進捗管理 * 社内外の関係者（グローバルチーム・CRO・ベンダー）との連携および調整 * プロジェクトのスケジュール・予算・リソース管理 * 臨床関連文書の作成・レビューおよび管理（TMF含む） * KPIを用いたパフォーマンスモニタリングと報告 * リスクの特定・対応策の策定およびエスカレーション対応 * 規制当局への提出資料関連業務のサポート * GCPに基づく品質管理および査察対応のサポート 理想の人材 * 製薬企業またはCROにおける臨床試験関連の業務経験 * 臨床プロジェクトの進行管理またはモニタリング経験 * ベンダーまたは外部パートナーのマネジメント経験 * 日本のGCPや関連規制に関する理解 * 英語を用いた業務遂行能力（グローバルとのコミュニケーション） 条件・待遇 * 各種社会保険 * 在宅勤務制度
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
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
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
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
JOB DESCRIPTION: MAIN RESPONSIBILITIES • Primary responsibility is ensuring implementation of quality plan at every stage of the Clinical Trial process/operations. • Implement quality assurance regulations. • Write and revise standard operating procedures. • Support and facilitate audits
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
Lead end‑to‑end operations in a global clinical laboratory organization Drive quality, people development, and continuous improvement initiatives Client Details * Global leader in clinical laboratory services, supporting pharmaceutical, biotechnology, medical, and healthcare organizations. * Providing a wide range of
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,