Position: Regulatory Affairs Manager, Japan Reports to: General Manager Location: Tokyo, Japan Purpose This role, reporting to the General Manager, is responsible for defining and executing the regulatory strategy for Japan. It involves overseeing product registrations and
Job Purpose The Medical Lead role is a unique opportunity for an experienced, innovative, and proactive medical professional to facilitate the understanding of the value of our medicines and vaccines, the science behind them and the public impact
Job Purpose & Key Responsibilities The Japan Head, Real-World Evidence & Health Outcomes Research will be the overall leader of the non-interventional data generation team for the Japan business. Accountabilities include management and development of a
Company Description 【This role is open for HKG Visa Sponsorship】 At Third Bridge, we’re a primary research business providing professional services to Private and Public Equity Investors, Investment Consultants, Investment Managers, and more. We help
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: Product Manager is responsible for the business of Rekovelle and Lutinus, which mainly includes but not limited to, development and implementation of a business plan and he/she does independently and/or with the support/under the
Job Description SummaryWith the Head of Patient Advocacy, drive the design and execution of an integrated patient advocacy strategy in Therapy Areas(TA) and Above Brand to create an optimal environment to foster relevant legislative and frame
Principal Responsibilities Critical responsivities of the head of Medical Information include, but not limited to, maintaining, and continuously improving the procedures and contents of Medical Information in ever changing industry environment in alignment with Alexion Global. Also, advancing
Primary accountability: Quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies) Proactive reporting of study-specific issues (including monitoring metrics) to the study team
At Dow, we believe in putting people first and we’re passionate about delivering integrity, respect and safety to our customers, our employees and the planet. Our people are at the heart of our solutions. They reflect
Primary responsiblity: Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP). Driving performance at
The Medical Science Liaison (MSL) is a field-facing role whose main objectives are to: exhibit a high degree of scientific and clinical knowledge, i.e. a robust knowledge of diseases, vaccinology, product development, clinical trials exhibit a high
Job Summary ・Support the development, alignment and execution of Patients Value Plan(PVP) for B one Health Mission in Japan (BHM-J) ・Provides the strategic solutions and framework (such as segmentation and targeting) for Post Fracture Care to
魅力:新薬上市にともない、チームが発足するため、チームビルディングはもちろん、MSLとしてのかなり上位の戦略に関与できます!●データ普及を加速させるために、外部の専門家や意思決定者が相互の科学的交流に従事する、現場で信頼できる科学的パートナーとなること。●治療領域における当社製品の科学的・医学的価値の理解を深め、明日からの医療イノベーションを加速させる最先端の科学的交流をもたらすことで新しい知見を収集する。メディカルサイエンスリエゾン(MSL)は、現場と向き合う役割で、主な目的は以下の通りです:当社製品の科学的・医学的価値に関する理解を深めるため、タイムリーで適切かつ頻繁に科学的な意見交換を行い、外部の主要な専門家から信頼される科学的パートナーとなる。募集企業の主要な医学的メッセージ、計画、将来の研究の強化に貢献するデータを収集し、医学的洞察を開発し、共有するためのステークホルダー関与計画を実行する。研究機会を特定し、批判的に評価するために、治療分野における医学的・科学的動向を常に把握し、実世界における当社製品の価値を高めるためのエビデンス生成計画の実行を支援する役割を果たす。患者、消費者、規制当局、支払者、医療提供者のニーズに対する理解を深めるための洞察を認識、記録、共有し、アンメットニーズの特定に向けて積極的に貢献する。社内関係者(メディカルアフェアーズ、メディカルインフォメーション、コマーシャルオペレーション)との効果的で適切なコミュニケーションを維持し、会社、業界、法律、規制の関連要件を完全に遵守する。すべてのガバナンスプロセスの優れた実行を確保することにより、業務理解とリスクマネジメントを実証する。The Medical Science Liaison (MSL) is field-facing role whose main objectives are to:■Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and
【応募要件】 臨床試験の経験は必須、企業経験(3-5年以上)があり開発経験があるMD(日本医師免許)保持者限定 経験によりClinical Science LeadもしくはSr. Clinical Scientistでの採用となる可能性あり Assume overall responsibilities as a regional/country level Development Team leader in the matrix setting to ensure alignment across key stakeholders and promote team work. Drive the development of Clinical
Company OverviewEmbark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. We are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as
Primary Purpose / Regulatory Responsibilities: The primary purpose of a Project Manager (PM) is to ensure and elevate the level of country operations to realize patient value by transforming company’s strategy into project delivery in Japan.
MAJOR ACCOUNTABILITIES • Report to the head of (Therapeutic Area) Medical Science • Maintain up to date scientific intelligence/clinical knowledge in relevant disease area(s) and provide appropriate strategic and operational input into UCB Strategies • Identify gaps
. MAJOR ACCOUNTABILITIES • Report to the head of (Therapeutic Area) Medical Science • Maintain up to date scientific intelligence/clinical knowledge in relevant disease area(s) and provide appropriate strategic and operational input into UCB Strategies Identify gaps
Job Description About This Role The person will be responsible for enhancing the company’s reputation in Japan by implementing pro-active communication tactics targeted towards multiple external and internal stakeholders. External stakeholders include media, industry, and general