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 ・FM-SOP、厚生労働省の医療用医薬品の販売情報提供ガイドラインなどの社内外の規制に沿った、SL/KDMとのScientific Exchange ・SL/KDMの依頼に応じた、最新科学情報、MISP等に関わる情報提供 ・Field Engagement Planに基づくIndividual Planの作成・実行 ・Scientific Exchangeを介したUnmet Medical Needs、Data Gap等のInsight収集 ・担当疾患領域に関わる論文、学会等の最新情報収集 ・SL Listの構築および更新 ・最新情報（Insight、論文情報、学会情報）の社内関連部署との共有 ・アドバイザリーボード、Medical Education等メディカルイベントのサポート Required Skills: Adaptability, Adaptability, Advisory Board Development, Clinical Knowledge, Clinical Medicine, Clinical Pharmacy, Data Analysis, Event Execution, Event
■ 職務内容 / Job Description 【Responsibility/Key Tasks 】 HEOR director is a leadership member of Evidence and Observational Research (EOR) and leading HEOR team as a head of HEOR. Accountabilities Establish HEOR organization and ensure
The Senior Medical Writer is responsible for planning, preparing, and managing medical writing projects as well as creating and reviewing documents in some instances. Reporting to the Head of Clinical Development Japan, the Senior Medical Writer is responsible for the
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
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Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation
Job Overview: A key operational role within our matrix organization, accountable for the clinical operational activities and performance within an assigned group of countries or delivery team, with responsibilities for customer connections and commercial activity. Leading
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
Fastly helps people stay better connected with the things they love. Fastly’s edge cloud platform enables customers to create great digital experiences quickly, securely, and reliably by processing, serving, and securing our customers’ applications as close
Job Description Why This Role? Why Now? Are you an enterprise technology professional seeking to elevate your technical career within an internationally supportive, customer-centric environment? Zendesk invites you to join our growing Tokyo team as a
We’re in an unbelievably exciting area of tech and are fundamentally reshaping the data storage industry. Here, you lead with innovative thinking, grow along with us, and join the smartest team in the industry. This type
“I can be myself at work.” You are more than a job title. We want you to feel comfortable doing great work and bringing your best, authentic self to everything you do. We value your talents,
【POSITION SUMMARY】 Greet guests and determine the number in their party. Seat guests by finding a clean, available table; pulling out chairs; placing clean/current menu in front of guest, etc. Guide guests through the dining rooms
１．主な職務における成果責任/ Description of Primary Role & Responsibility A. 市販製品・治験薬の安全性情報（有害事象）収集、評価 / Collection and Assessment of safety information (adverse event information) of marketed/investigation Pfizer products B. グローバル安全性データベースへのデータ入力と管理 / Data entry and management on Global Safety Database C. 日米欧の法規制の遵守、安全性コンプライアンス維持
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
1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective therapeutic/disease area
PGIMリアルエステート・ジャパンにて、 主にトランザクション、アセットマネジメントに関わるインターンを募集します。トランザクション、アセットマネジメントの他、投資リサーチ、クライアントサービスなど、幅広い業務をサポートしていただきます。 ※詳細は下記英文の募集要項をよくお読みください。 応募資格 日本でフルタイム就労が可能な方（Japan Citizenshipをお持ちの方） 現在大学3年生以上の、大学・大学院生の方 GPA 3.5以上 日本語：中級〜上級レベル必須（読み・書き・会話） 英語力：中級レベルあれば尚可 Excel（必須）、PowerPoint／Wordの基本スキル 異文化環境でのコミュニケーション力をお持ちの方 勤務条件 期間：9-12月の間に、３か月間勤務可能な方。その他の時期は募集していません。 勤務時間：9:30〜18:30（月〜金）、パートタイムではなくフルタイム勤務 勤務地：東京都千代田区永田町（プルデンシャルタワー） 選考について 添付いただくカバーレターまたはレジュメに、Japan Citizenshipの有無・希望する就労期間（日付含）を明記してください。 書類選考は随時実施 定員に達し次第、募集終了 A GLOBAL FIRM WITH A DIVERSE & INCLUSIVE CULTURE: As the Global Asset Management
About us At Sierra, we’re creating a platform to help businesses build better, more human customer experiences with AI. We are primarily an in-person company based in San Francisco, with growing offices in Atlanta, New York,
As a global leader in cybersecurity, CrowdStrike protects the people, processes and technologies that drive modern organizations. Since 2011, our mission hasn’t changed — we’re here to stop breaches, and we’ve redefined modern security with the