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Regulatory Agencyの求人-東村山 - 77 Job Positions Available

1 – 20 of 77 jobs
Alexion Pharmaceuticals jobs

This is what you will do: The Senior Manager, Regulatory Affairs-Chemistry, Manufacturing, and Controls (RA- CMC) in Japan will manage complex projects for CMC submission in Japan and responses to regulatory agency inquiries for Alexion’s commercial and investigational products.

Alexion Pharmaceuticals  27 days ago
GSK jobs

Responsibility: 変更提案に対する薬事影響評価(変更カテゴリ―、必要なデータ)の特定 市販製品(低分子医薬品及び/又はバイオ医薬品)の変更管理における薬事的なリスク低減策を含むCMC薬事戦略の立案・実行支援 薬事アクション(一変・軽変・相談・照会回答)に供する高品質な資料の適時作成 海外関連部署に対する本邦規制要件の提示・解説 (担当マネージャー)チーム成果物(提案・資料等)の品質保証(整合性、適切性) Role: 製造所の変更提案に対し適時薬事影響評価を行う。 市販製品の薬事アクション(一変・軽変・相談・照会回答)に対し、提言、方針策定の支援、海外を含む関連部署との交渉を行う。 薬事アクション(一変・軽変・相談・照会回答)に供する資料につき、海外薬事を含む国内外の品質部門と協働して資料作成を行う。 他部署との協業上の問題(役割分担等)の解決・調整を支援し、プロセス改善に寄与する、あるいはその提言を行う。 (担当マネージャー) チームメンバーの上記活動に対する能力開発を含めた指導・支援を行う。 関連部署との個別の課題/問題につき、必要な調整・解決のための協議を行う。 ※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。 Basic Qualification スキル Skill 分析化学、製剤・薬剤学・プロセス工学(特に製造方法あるいはGMP)等に関する知識 品質に関わる国内規制、各種ガイドライン及び日本薬局方などの知識 ロジカルシンキング(論理的に物事を整理し、本質を見極められる) 他者との緊密な協力関係を構築し、協業できること Word、Excel、PowerPoint、Outlook、 経験 Experience CMC関連業務(分析、製造、QA、CMC薬事など、関連業務5年以上が望ましい) CMC薬事経験必須、スタッフは関連業務経験の有無により以下を考慮することがある - 変更管理業務を含むCMC薬事への興味の高さ・習得意志の強さ - 業務に利用可能な傑出したスキル(例:英語がnative levelなど)またはコンピテンシー(自己認知・成熟性、変革行動、顧客志向性など)を1つ以上有する 学位/資格/語学力 Education/certification/Language 医学、薬学、生物学、物理科学等での学士もしくはそれと同等以上

GSK  22 days ago
CSL jobs

The Team Lead, Global Regulatory Affairs CMC - Japan is responsible for providing strategic leadership and operational oversight for the Global Regulatory Affairs CMC - Japan team. Reporting to the Head of Global Regulatory Affairs CMC you will partner

CSL  18 days ago
Meta jobs

Meta is seeking a Partner Manager who will serve as a critical relationship manager to government, political, and advocacy (GPA) partners utilizing our commercial products. In this role, you will establish and strengthen key partner relationships

Meta  15 days ago
Stryker jobs

Work Flexibility: Hybrid or Onsite Key Areas of Responsibility: Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies Participates in advocacy activities of a more advanced technical and/or tactical or strategic nature

Stryker  3 days ago
GSK jobs

Role Purpose: To strengthen execution capability within the brand team and ensure high-quality and timely delivery of key marketing initiatives. Key Responsibilities: Lead end-to-end execution of marketing initiatives (promotional materials, digital content, campaigns) Plan and execute

GSK  27 days ago
Syneos Health jobs

Principal Biostatistician / Programmer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our

Syneos Health  27 days ago
Allianz jobs

Join us now as Sales Manager in Japan within the Japan Retail Sales, Distribution AP. In this role, you will be responsible for creating the documents which the outsourcing service provider provides for AGI Japan collaboratively,

Allianz  27 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  28 days ago
MSD jobs

Job Description ・医薬品開発戦略に対して、臨床薬理/ファーマコメトリクスを活用した提案を行い、早期承認に貢献する ・他チームや臨床現場に対して、治験薬の臨床薬理学的情報を的確に提供するとともに、問題解決を行う ・プロトコールの試験デザイン・被験者数・解析方法並びに試料のサンプリングポイントなどを検討し、適切な提案を行う ・薬物動態(PK)解析を実施し、治験総括報告書の該当するセクションを作成する ・PK結果の速報を作成し配信する。 ・臨床現場に提供すべき治験薬の臨床薬理/薬物動態学的情報を精査し、非臨床ADMEを含む申請資料の臨床薬理関連部分に過不足無く盛り込む ・臨床現場に提供すべき治験薬の臨床薬理/薬物動態学的情報や用法・用量に関連する臨床薬理領域の電子データを特定し、戦略に応じて、適切に提出する ・PMDA相談の資料作成・当日の議論に臨床薬理担当者として加わり、承認に貢献する ・本社の担当者と継続的に連絡を取りながらこれらの業務を進める。 ・必要に応じてモデリング&シミュレーション(M&S)を実施する ・グループ内のM&Sスキル向上への提言及び下位部員に対するメンターとして教育・指導的役割を担う 応募条件 【必須(MUST)】 ・臨床薬理部門もしくは関連部門での3年~10年程度の実務経験 ・M&S(population PK, PK-PDまたはExposure-Response解析)の知識・理解 ・非臨床ADMEの知識・理解 ・ノンコンパートメントPK解析の知識・理解 【歓迎(WANT)】 ・ノンコンパートメントPK解析の実務経験 ・M&S(population PK, PK-PDまたはExposure-Response解析)の実務経験 ・各品目のプロジェクトチーム内で、他のメンバーと積極的に関わって議論/プレゼンできる方 ・海外の担当者とのメール、電話等でのコミュニケーションが可能で、関係を構築できる方 ・CDISC / non-CDISCの電子データ申請に関する基礎知識・経験があれば尚可 ・博士号(PhD)であれば尚可 Required Skills: Clinical Trial

MSD  25 days ago
GSK jobs

Job Purpose At GSK, we unite science, technology, and talent to get ahead of disease together. Our goal is to improve the lives of billions across the world. By bringing together outstanding people in an inclusive

GSK  23 days ago
Dexcom jobs

The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock

Dexcom  23 days ago
Apex Group jobs

The Apex Group was established in Bermuda in 2003 and is now one of the world’s largest fund administration and middle office solutions providers. Our business is unique in its ability to reach globally, service locally

Apex Group  23 days ago
New Relic jobs

We are a global team of innovators and pioneers dedicated to shaping the future of observability. At New Relic, we build an intelligent platform that empowers companies to thrive in an AI-first world by giving them

New Relic  21 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 days ago
PSI CRO jobs

Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials

PSI CRO  21 days ago
GSK jobs

Position SummaryYou will lead health technology assessment (HTA) and evidence synthesis activities to support access and reimbursement in Japan. You will work with cross-functional colleagues in market access, clinical development, regulatory, and global HEOR teams. We value

GSK  21 days ago
Takeda jobs

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms

Takeda  21 days ago
LSEG jobs

ABOUT US: LSEG (London Stock Exchange Group) is more than a diversified global financial markets infrastructure and data business. We are dedicated, open-access partners with a commitment to excellence in delivering the services our customers expect

LSEG  17 days ago
Motorola Solutions jobs

Company Overview At Motorola Solutions, we believe that everything starts with our people. We’re a global close-knit community, united by the relentless pursuit to help keep people safer everywhere. We build and connect technologies to help

Motorola Solutions  17 days ago

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