Job Title Regulatory Affairs Senior Manager - IGTD Job Description Regulatory Affairs Senior Manager Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more
Responsible for planning and executing medical activities and make sure timely and effective execution aligned to medical strategy. Reporting to TA Medical head 1. Key accountabilities 1-1. Lead Medical Strategy ■ Lead and monitor the execution
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 Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue over $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer.
職務の目的および主な業務内容 Job Purpose & Key Responsibilities 職務の目的 The Japan Medicine Development Lead (J-MDL) is accountable for a medicine development in Japan to ensure delivery differentiated medicines of value for patients, stakeholders and markets in Japan. The
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health
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
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials
Görev Tanımı The Position The Pharmacovigilance Senior Specialist (PV Senior Specialist) will be a part of Regional Regulatory Affairs and affiliate Pharmacovigilance organization and reporting into the head of Japan Pharmacovigilance. The PV Senior Specialist is
Work Flexibility: Hybrid or Onsite Basic purpose of role/Why the job exists: The Transport Product Engineer is responsible for the day to day product support and technical aspects of customer product enquiries. In partnership with the
【募集Summary】 RM(Records Management Manager)は、IQVIAにおけるTMF Managementにおいて、Global及び顧客のPOC(Point of Contact)として、ProjectのManagementを実施します。また、臨床チームと協働で、TMFの手順構築、KPIのOversight、各種Issue発生時のCAPA対応等を通して、Inspection Readyな状態を保てるようSupportします。 我々のRecords Management Teamは、IQVIAにおけるTMF managementをGlobalと協働で、centralで実施しております。またIQVIAのＲＭの強みとして、Dx化を促進し、AIも導入、効率的かつ標準的なTMF Managementプロセスを取り入れております。新薬の承認取得に向けたEvidence確保のため、私たちと一緒に働きませんか？ 【業務内容】 ＜Portfolio Lead＞ ● RMのSPOC(Single Point of Contact)として、ProjectのIssue management, escalationを実施する。 ● TMF業務のEAC forecastを提供し、Projectをサポートする。 ● 適切なリソース配置とUtilizationを適切にする。 ● RMとCL/PL間でコミュニケーションをとり、スポンサーおよび試験の状況のupdateを定期的に提供する。 Audits and Inspections時、質疑応答、PLをサポートする。 ● TMFに関するCustomerの要求に関して、CSMGの担当者とコミュニケーションをとる。 ● 必要に応じて、カスタマーのTMF窓口とコミュニケーションをとる。 ● 必要に応じて、パートナーシップとしてのTMF管理遂行をサポートする。 ●
Cochlear is the global market leader in implant hearing solutions. Cochlears mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear
