Title: Medical Advisor / Medical Scientific Liaison FOP Company: IPSEN K.K. Job Description: As part of the Medical Affairs department, the MA/MSL is a hybrid, field-based scientific expert to external and internal stakeholders delivering non-promotional information
Job Description Main Responsibilities: Support the Quality Assurance activities of the Marketing Authorization Holder as described below: Ensure the implementation of GQP Quality Assurance activities and ensure activities operate within established policies/procedures, global requirements, and all
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
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
■ 職務内容 / Job Description Lead Safety Information Management Group to manage pharmacovigilance activities incl. collecting, evaluating, and submitting safety information to relevant parties (e.g. PMDA, AZ global Patient Safety, licensing partners) and lead communication (incl. inspection
This is what you will do: The Medical Affairs Associate Medical Lead prepares a medical plan, which serves as the basis of medical activities of Alexion Pharma GK (AP-J) as a whole, and carries it out
【職種】治験関連 製造販売後調査（PMS）の契約書式の作成に関する業務、主には次の通り： - PMS契約書式の作成に関するPMS業務担当者への説明・指導 - PMS業務担当者により作成・提出されたPMS契約書式の内容確認（内容確認後のフィードバックも含む） - PMS契約書式の社内捺印処理及び配送 - PMS書式（締結済、締結段階の最終版）の保管管理 - PMS書式の更新業務 - 前述のPMS契約書式の作業着手から作業完了までの進捗管理 その他、付帯する庶務業務（Pharmacovigilanceチームに対するアドミサポートを含む） 日比谷駅直結（千代田区／最寄り駅：日比谷駅、有楽町駅、乃木坂駅） 9：00-18：00 【派遣先について】 アメリカ本社の製薬会社 規模50名程度 業種：医療・介護関連 【派遣会社】マイケル・ペイジ・インターナショナル・ジャパン株式会社 ●各種社会保険 ●有給休暇 ●交通費支給（案件により）...
* 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
* The Safety Management Officer will oversee all safety management and pharmacovigilance (PV) activities in Japan. * This role involves ensuring compliance with local regulations, managing risk, and maintaining high standards of safety for all products. Client
