ジェンマブは革新的な抗体医薬の開発に注力し、患者さんの生活を改善することに力を尽くしています。 私たちは、extra[not]ordinary® な未来を共に築くことを使命とし、革新的な抗体製品の開発や人々を感動させる抗体医薬品で、がんやその他の深刻な病に苦しむ患者さんの生活を根本的に変え、治療の未来を切り拓いています。 ジェンマブは思いやりがあり、率直で、患者さんに貢献したいという強い思いを持った人たちがともに働き、科学に基づく変化をもたらします。大胆さと高潔性を持って行動し、新しい未来をつくることを目指すこと が、この使命を果たすために不可欠だと信じています。 私たちは大きな志を掲げ、楽しく、そして思いやりの心を忘れずに、日々意義のある仕事に取り組んでいます。私たちは、個々のユニークな貢献を受け入れ、それらを原動力として、患者、ケアパートナー、ご家族、そして社員のニーズを満たす革新的なソリューションを生み出し、育み、維持するグローバルな企業文化の構築に努めています。 私たちの想いに共鳴し、自分らしく活躍できそうだと感じたら、ぜひ一緒に働きましょう。 Position Summary: The Medical Affairs Strategy Scientist (MASS) will lead the planning, coordination and execution of the designated product(s) launch for Genmab medical affairs department in collaboration with Medical Affairs Strategy Lead (MASL). MASS will
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Typical Accountabilities - Respond directly to complex or escalated medical information inquiries by leveraging advanced knowledge of assigned products, therapeutic areas, and company protocols. - Prepare and maintain comprehensive, up-to-date information packages, resource materials, and documentation for
Typical Accountabilities- Respond directly to complex or escalated medical information inquiries by leveraging advanced knowledge of assigned products, therapeutic areas, and company protocols.- Prepare and maintain comprehensive, up-to-date information packages, resource materials, and documentation for assigned products
MAIN RESPONSIBILITIES / DUTIES JOB POSITION PURPOSE • Act as the Amyloidosis team lead and line manager, leading a team of MAS. Shape the local strategy and ensure the delivery of scientific‑medical expertise and exchange with leading
【Job Description】 The Director Oncology Corporate Affairs is a central point of counsel and corporate affairs insight for AstraZenecas Oncology Business in Japan. This role is responsible for defining and advancing policy interests aligned to AstraZenecas ability to
As the Manager, Global Regulatory Affairs CMC, you will shape CSLs regulatory CMC strategy in Japan, partnering across Global Regulatory Affairs, R&D, Manufacturing and local business teams to support the development, registration, commercialisation and lifecycle management of our
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Administrative Coordinator to join our Regulatory Affairs team, supporting our Japan Regulatory Affairs organization
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Regulatory Strategy Oncology & Japan Affairs to join our Regulatory Affairs team,
企業概要 About AbbVie 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
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.
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
CSL Behringは、希少疾患・重篤疾患の患者さんに革新的な治療法を届けるグローバルバイオ医薬品企業です。私たちは「患者さんにより良い治療の選択肢を届ける 」という使命のもと、イノベーション、コラボレーション、そして患者さん中心の価値創造を推進しています。 このたびMedical Affairsチームでは、Medical Science Liaison（MSL） を募集しています。 本ポジションはField Medical Leadにレポートし、免疫グロブリン（IG）を中心とした免疫疾患・神経免疫疾患・血液疾患領域において、医学専門家との科学的パートナーシップを構築しながら、Medical Strategyの実行と患者さんへの価値提供を推進いただきます。 Your Role 医学専門家との関係構築・科学交流 KOLや医療従事者（HCP）との長期的な信頼関係を構築し、科学的交流を推進する 医学・科学情報に関する窓口として、適切かつタイムリーな情報提供を行う 医学的インサイトを収集し、患者さんへの価値創出につなげる 医学戦略の推進 ブランドチームおよびクロスファンクショナルチームと連携し、Medical Strategyの策定・実行に貢献する 医療現場から得られる知見を組織へ共有し、製品ライフサイクルマネジメントを支援する エビデンス創出・研究支援 Scientific Advisory Board、学会、医学教育プログラムの企画・運営を支援する Investigator Initiated Study（IIS）や共同研究、臨床試験関連活動をサポートする データギャップの特定およびエビデンス創出活動に貢献する 治療領域エキスパートとしての役割 Immunoglobulinおよび関連疾患領域における高度な専門知識を維持・発展させる 最新の医学情報や競合環境を継続的に把握し、社内外へ知見を提供する Scientific TrainingやEducation活動を通じて知識共有を推進する Your Skills and Experience MSLとしてのご経験、もしくはMedical Affairs、Clinical Development等のメディカル機能における経験 免疫グロブリン領域に関する知識・経験、または免疫・神経免疫・血液疾患領域におけるバックグラウンド
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
企業概要 About AbbVie 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
EP & Transplant Medical Head Location: Japan About the job As EP & Transplant Medical Head within our General Medicines team, youll provide senior strategic leadership across kidney transplantation and our established portfolio, empowering the team and driving
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
Work Flexibility: Hybrid or Onsite 職務内容 マネジャーの最小の指導の下、薬機法全般についての知識と経験を有し、円滑な薬事申請及び関連業務の遂行を目的とする。 Under minimum supervision by Manager and Lead Specialist, he/she understands the laws and regulations, and efficiently conducts the duties such approval applications, notifications and other related tasks. Key Activities