Who We Are At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward – always pushing ourselves
Job title – Associate Manager, Engineering/SHE, Taste Location – Ibaraki, Japan Job model – On Site To lead and operationalise Safety, Health, Environment and Security (SHE&S) management system to improve on SHE&S awareness and culture at Kitaibaraki
JOB DESCRIPTION: MAIN PURPOSE OF ROLE Implement quality standards, ensure and execute compliance on every stage of the process. MAIN RESPONSIBILITIES Develop and implements quality assurance strategies and regulations. Assesses potential risks, ensures compliance and gives
For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases
J.P. Morgan is seeking a bilingual (Japanese and English) Supervisory Analyst (SA) to join its APAC SA team, which consists of 21 SAs based in Asia Pacific, Europe, and North America, providing 6-day, 24-hour coverage for
Quality Operations Process Improvement Associate - VIE Contract Location: Tokyo, Japan Target start date: 01/07/2025 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between
You will be responsible for: Quality professional with strong subject knowledge, both in depth and breadth. Experience from a number of different areas of quality. Will control, monitor and develop systems and procedures to enhance the
＊スペシャリティ・ジェネラルメディスン領域での開発薬事業務及びスペシャリティ・ジェネラルメディスン薬事部（SGMRA）/オンコロジー・ワクチン薬事部（OVRA）の両部横断的な活動業務及び人財育成をリードする役割を担当していただきます。 新薬の承認取得を通して、日本の患者さんにイノベイティブな治療を提供することに貢献できる業務です。 新薬開発及びライフサイクルマネジメントにおいて、薬事戦略を立案/実行する。 薬事関連規制や関連する事例等を考慮した薬事戦略を立案し、チームメンバーと協働して実行する。 承認申請や対面助言等、薬事関連業務をリードし、規制当局との交渉戦略を立案/実行する。 薬事的課題を分析し、適切な解決策を提案/実行する。 海外チームと良好な信頼関係を築き、薬事関連規制や薬事戦略の提供を実行する。 海外薬事規制等を踏まえた国内薬事規制の問題点を提示する。 規制当局と良好な信頼関係を築き、適切なコミュニケーションと薬事的交渉を実行する。 規制当局との交渉の場において議論内容をリードする。 上記業務のほか、SGMRA及びOVRA両部横断的な活動業務及び人財育成をリードする（例：Hyper acceleration, GRA Japan/China Focus Group, Japanese Regulations Training for GRA等）。 SGMRA及びOVRA両部横断的な活動において、戦略構築における各担当者に対するアドバイスを含む、担当プロジェクトを成功させるために必要な支援を提供する。 Line Managerと共に他のSGMRA及びOVRA担当者の業務に関するアドバイス及びメンタリングなどによりSGMRA及びOVRA各担当者の成長を支援する。 ※職務内容および勤務地の変更範囲は会社の定めるところとする。 必要な条件Basic Qualification スキル Skill 薬機法の体系、開発・承認審査の概略に関する知識 プロジェクトチームや規制当局で開発薬事戦略を説明するコミュニケーション力 グローバルコミュニケーション力（英語での理論構築、読み・書き・会話力） 難易度の高いプロジェクトや国内外ともにステークホルダーが多いプロジェクトであっても、プロジェクトチーム内外のステークホルダーとの調整を遂行するスキル 高難度のプロジェクトにおいても薬事が主担当となる業務を超えて担当プロジェクトチームをリード/サポートすることができる高度な、リーダーシップスキル 経験 Experience
Job Description Summary The Senior Statistical Programmer is responsible for all statistical programming aspects of assigned studies or project-level activities. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-development plans in Novartis
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.
Overview Company: Kakoo Services LLC Location: Kadena Air Force Base Pay: $32/hr - $37.88/hr + Health & Wellness $4.22/hr worked (in lieu of benefits) Benefits: Vest vacation, sick leave, holiday leave, Life, Accidental Death and Dismemberment,
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Job Description Summary The SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies
■ 職務内容 / Job Description Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in
Job Description Summary The Study Leader is the leader of the cross-functional clinical trial team (CTT), guides planning andmanagement of the assigned clinical study/studies end-to-end to achieve Global Program Team(GPT), Global Clinical Team (GOT) and GCO
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Our story Strada is a technology-enabled, people powered company committed to delivering world-class payroll, human capital management, and financial management solutions to organizations globally. With a team of more than 8,000 experts and over 30 years
For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases
JOB DESCRIPTION Job Title: Contract Associate, International Legal Department Department / Cost Center: 861 Legal Reports to (Job Title): Associate Director, Head of International Contract Management Job Code: Location: Tokyo, Japan Date Prepared: January 24, 2025 Full-Time Part-Time
The Associate Director, Product Owner is accountable for designing and delivering the digital & technology roadmap in support of GSK Japan Development and Regulatory Affairs organizations to achieve key business strategies including simultaneous development and simultaneous submission. The
