Are you passionate about improving patient outcomes? Do you have experience in medical affairs and a desire to make a difference in the healthcare industry? We are looking for a Medical Advisor to join our dedicated
Job purpose Medical Science Liaison (MSL) is a field-based role in the new Medical and Development organization, reporting to MSL Head. In order to build a trust with External Experts (EE) and scientific community through, MSL
Manage Safety staff responsible for Safety Operations processing in alignment with departmental and corporate standards. Contribute to Global initiatives. Work in close collaboration with SM and other relevant stakeholders supporting the achievement of local and global
Job Profile SummaryJob Overview Responsible for management and service delivery excellence for assigned projects, covering single or multiple Lifecycle Safety functions (clinical trial and / or post-market). Provide leadership and accountability for customer-facing activities and oversight of
部門機能 •IQVIAの豊富なセカンダリーデータ分析とプライマリー・マーケティング・リサーチ(PMR)を、世界各国のベストプラクティスに基づく独自の調査分析手法によって行い、R&D～上市後までの製品ライフサイクルの幅広い課題に対する施策やマーケティングプランのPDCAをフルサポート。 業務内容 •プライマリー・リサーチを中心とするマーケティング・リサーチャーとして、医療・医薬品・医療機器等に関するプライマリー・リサーチ事業の運用を担当（将来的には、新サービスの企画をご担当いただくことも想定） ※国内外のクライアントに対し、プライマリー・リサーチ・プロジェクトの企画立案・設計～レポートまでの全工程を担当 ※特に、レポート作成段階では、調査結果の集計・分析、および、クライアントの課題解決に貢献できるような示唆出しをリード 応募要件 下記のようなスキルアップ、キャリアアップに興味がおありの方は是非ご検討ください！ 1. 医療・医薬品の知識があり、マーケティングリサーチのスキルを磨きたい ・【マーケットリサーチ全体のスキル】調査設計から、調査、分析、レポート作成全般のスキル習得が可能です ・【ロジカルに考える力】調査設計～レポート作成を通して、仮説抽出～検証、ロジカルに考え書く力を身に着けます ・【データ分析力】単純な集計から統計分析、分析結果から潜在ニーズや課題を読み取る力を養います 2. リサーチ経験があり、ヘルスケア業界で貢献したい 【以下の方歓迎】 •医療・医薬品・医療機器業界で、MRや薬剤師の経験がある方•医療・医薬品・医療機器業界でのリサーチまたはコンサルティングの経験がある方•社会心理学やマーケティングの勉強をしてきた方•統計分析 IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
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.
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
Do you enjoy working as an Executive assistant to the C-level office? Are you interested in utilizing both Japanese and English at a global company? About our Team Elsevier Health applies innovation, facilitates insights, and helps
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.
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
■職務概要 一般的な作業指示者の下で、適用される地域および/または国際的な規制要件、標準作業手順(SOP)、プロジェクト要件、および契約上のガイドライン/予算ガイドラインに従って、Site Activationの業務に関連する治験参加国レベルの業務を実施します。 メンテナンス作業も含まれる場合があります。 ■職務詳細 一般的な作業指示者の下で、必要に応じてSite Activation Manager (SAM)、プロジェクトマネージメントチーム、およびその他の部門と緊密に連携しながら、適用される規制要件、SOP、および作業指示に従って、アサインされた試験の治験実施施設のSite Activation活動を実行します。 上級スタッフの指導の下、規制文書の作成と完全性、一貫性、正確性を確認、QCを実施します。 各治験実施施設の治験関連文書および契約文書の完成をチームメンバーに通知します。 完成したドキュメントを治験実施施設や社内のプロジェクトチームのメンバーに配布します。 社内システム、データベース、治験管理システム、タイムライン、プロジェクトの予定の更新とメンテナンスを実施し、正確で完全なプロジェクトの管理情報となるためのサポートをします。 進捗状況、文書の承認と実行、規制要件、倫理、同意説明文書(ICF)、Investigator Pack (IP) release documentsの内容のレビュー、進捗管理、フォローアップします。 ■必須経験 事務的職種での3年の経験、または同等の教育、トレーニング、経験。 細部まで取り組む業務処理能力と複数プロジェクト管理能力。 優れた文書処理とMS Officeアプリケーションの知識。 優れたコミュニケーション能力。同僚、マネージャー、スポンサーとの効果的な仕事上の関係を確立し、維持する能力。 IQVIA is a leading global provider of advanced analytics, technology solutions
International SOS is the world’s leading medical and security services company with over 12,000 employees working in 1,000 locations in 90 countries. International SOS Government Services administers the TRICARE Overseas Program providing high-quality, accessible health care
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.
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
Are you interested in improving the lives of millions of people, contributing to a company that works with innovation and is a pioneer in antidiabetic drug? If yes, this position of Senior Medical Advisor for diabetes
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.
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.
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.
