* At the front line of communication with stakeholders at hospital sites / clinics, youll manage clinical aspects of full-service global trial projects. Your responsibilities will include ensuring timelines, targets, and standards are met for clinical research projects spanning
Job Description The position takes a responsibility for medical contents in all clinical development programs in assigned therapeutic areas (such as dementia, movement disorders, neuromuscular, and MS/Immunology etc.) in Japan. The individual functions as a scientific and
Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core
Job Title CT Clinical Scientist Job Description Job title: CT Clinical Scientist Key Areas of Responsibility 1.Identify and connect new customer needs, solutions and technologies to initiate new methods (or disruptive enabling technologies) of diagnosis, treatment and/or care
Do you have a strong background in non-clinical activities? We are looking for a Non-Clinical Expert to join our team at Novo Nordisk. If you are ready to contribute to the development, submission, and approval of new drugs/devices,
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.
* Lead and project management of the following studies: - CSS (Company-led research) - IIS (Doctor-led research) - Collaborative study - Including oversight of external CRO Client Details * Leading global CRO business, with rich project pipeline in
* This position will be responsible for managing assigned clinical studies globally and locally, overseeing study activities, budgets, timelines, and vendor relationships. * The role involves leading a multifunctional team, ensuring adherence to regulatory requirements, managing study
Job Description The position takes a responsibility for medical contents in all clinical development programs in assigned therapeutic areas (such as dementia, movement disorders, neuromuscular, and MS/Immunology etc.) in Japan. The individual functions as a scientific and
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
ROLE SUMMARY The Platform: The Chief Medical Affairs Office’s RWE Partnerships and Platforms organization is responsible for establishing global RWE data and scientific leadership through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic
Job purpose: Responsible for implementing the Medical Affairs Plan of specified Team strategies, driving a consistent approach to carrying out scientific engagement activities internally and in the field; ensuring compliance with all relevant regulations and GSK
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
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
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
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. We
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
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
