Job Title Regulatory Affairs Senior Specialist Job Description Job title: Regulatory Affairs Senior Specialist Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier
Requisition #: 15621 Our Mission: Powering Innovation That Drives Human Advancement When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
General Information Job Advert Title: Senior Manager, Technology and Data QA Location: Nihonbashi, Tokyo Division: Quality Assurance Employment Class: Permanent Description 【Purpose & Scope】 Responsible for managing and executing the Technology and Data Quality Assurance (TDQA)audit
Requisition #: 15621 Our Mission: Powering Innovation That Drives Human Advancement When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more
Job TitleRegulatory Affairs Manager Job Description Job title: Regulatory Affairs 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 sustainable
No Agency Submissions Accepted. Location: Tokyo, Japan 100% remote Onwards Together! Illumio, the pioneer and market leader of Zero Trust segmentation, prevents breaches from becoming cyber disasters. Illumio protects critical applications and valuable digitalassets with proven
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
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.
At Amazon we develop devices to enrich our customers’ daily lives through features and services that entertain, inform, and make everyday tasks easier. We continually innovate on behalf of customers, and we pursue the invention and
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.
The Open Research Support Specialist supports authors with all customer service queries related to Open Access (OA) publishing, in close consultation with the Journal Editorial Office, Finance, Production teams and the Open Access Policy teams at Springer
Basic purpose of the job To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization. Accountabilities ・Strengthen
Requisition #: 15259 Our Mission: Powering Innovation That Drives Human Advancement When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more
Requisition #: 15259 Our Mission: Powering Innovation That Drives Human Advancement When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more
Work Flexibility: Hybrid or Onsite Who we want: • Hard-working winners. Confident, competitive and results-oriented professionals who create a track record of success. • Dedicated achievers. People who thrive in a fast-paced environment and will stop
製品: 今日の臨床サポート：医師向けオンライン製品 プロシージャ―ズ・コンサルト：臨床従事者、医学生向けオンライン製品 業務内容: 医師が臨床現場で治療方針を決定する際に参照するオンライン二次文献データベース「今日の臨床サポート」のコンテンツを更新する コンテンツを最新の医学エビデンス、診療ガイドライン、その他の臨床情報ソースに基づいて最新の状態に保つ 医師である著者や監修により執筆／改訂されるコンテンツを編集する 校正者やベンダー、ライセンス担当者、その他の編集スタッフと協同してコンテンツを継続的にメンテナンス／公開する 薬剤師と協同して薬剤情報を更新する マーケティング、セールス、テクノロジーチームとも協同する サブリードとして、企画の管理進行およびメンバー育成を行う その他のアサインされた責務やタスク等を遂行する 必要となるスキル・経験 編集業務の経験 ビジネス初級以上の英語力 英語の文章を読むことに抵抗がないこと 英語の簡単な文章が書けること Microsoft Word、Excel、PowerPointに関する基礎的なスキル 歓迎するスキル・経験 医学医療出版物（オンライン記事）の編集経験 医療資格（看護師、薬剤師） メディカルライター チームリーダー 求める人物像 締め切り/スケジュールへの意識が高く、複数の業務を同時並行して優先順位を付けながら取り組める 未経験のことでも前向きに吸収しながら取り組める ・・・・・・・・・・・・・・・ Product: 1. Todays Clinical Support: An online product
Role summary Lead or support the analysis, adaptation, creation, and distribution of top-tier Health Economic and Outcome Research (HEOR) to promptly achieve the best possible reimbursement and pricing for Pfizer products and/ or to enhance their
Job Description SummarySite relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country in adherence
Our Company Changing the world through digital experiences is what Adobe’s all about. We give everyone—from emerging artists to global brands—everything they need to design and deliver exceptional digital experiences! We’re passionate about empowering people to
