At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Pharmacovigilance Reporting Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape
At Regeneron, our medical affairs physicians and scientists are at the forefront of innovation, playing a crucial role in our global development organization. As a key liaison between Regeneron and the scientific and healthcare community, you will
Our medical affairs physicians and scientists are experts on our medicines and form a valuable part of our global development organization including Regeneron Japan KK. We serve as an important liaison between Regeneron and the scientific and
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
Job Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and
Key Account Manager – Oncology Japan At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming
部門：安全性部門 Product Specialist メインの業務内容： 顧客から新規案件についてRFP ( Request for Proposal ) を受領したら、見積書と提案書を作成する役割。 その他状況により、PM的な役割も担っていただく。 必須経験：PV経験5年以上 、英語スキル （英語面接が最終面接） Job Overview Accountable for management and service delivery excellence of a range of large sized regional and global projects as assigned,
About us BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline
Basic purpose of the job* The Head of Development Regulatory Affairs 1 or 2 has responsibility to develop and implement regulatory strategy for the assigned therapeutic areas (TAs) and exercises activities which include: Guide subordinates on the
Duties & Responsibilities ベーリンガーインゲルハイムの重点疾患領域であるメンタルヘルス領域では，まもなく上市する予定の薬剤を含めた複数のパイプラインを有しております。そのため，開発段階から上市後まで幅広くメディカル活動をリードするMA（Medical Advisor）を必要としています。グローバル戦略に沿い，複数の部署を横断するチームメンバーと協働しながら，エビデンス構築，専門家からのインサイトに基づくアンメットメディカルニーズの特定，アドバイザリーボード会議等の企画立案を責任者として担う役割です。この中で、日本の意見はグローバルの戦略に組み込まれますので、非常にやりがいのある仕事です。また、ドイツ本社メンバーとの国際会議や海外学会への参加など、海外のステークホルダーとのコミュニケーションも役割の一つです。 国内におけるメンタルヘルス領域のアンメットメディカルニーズを理解し，臨床研究の基本的な知識とプロジェクトを適切にマネージする能力，また他部署とのコラボレーションや外部専門家（External Experts）とのコミュニケーション，アドバイザリーボード会議や承認後の薬剤の価値最大化・適正使用に必要なメディカル戦略も検討していく長期的な視野を持った人材を求めています。また、ピープルマネージャーとして、タレントマネージメントの一環として、メンバーのキャリアプランを作成し、コーチングを含む必要なサポートを提供します。さらに、マーケティング部門などと組織横断的なコラボレーションを率先し、実践いただきます。 Jop profile for Medical Advisor: In Mental Helath Therapeutic Area of Boehringer ingelheim, we have multiple pipelines including a product will be launched shortly for this field. A Medical
Basic purpose of the job Delivers project management support to the asset team and next–level teams with the focus on asset strategy execution and asset progress. Coordinates the interactions with all key stakeholders, local and Global
Basic purpose of the job Independently writes and manages clinical documents, such as clinical trial reports, Investigation Brochures, Protocols and briefing documents, in both local and global cross-functional project- and study teams, as well as local clinical regulatory documents
Basic purpose of the job HEOR Manager or Senior Staff will be responsible for and lead the development and implementation of the evidence generation strategy to maximize Boehringer Ingelheim asset value and optimize access to medicines through
1. Basic Purpose of the Position In order to develop veterinary biological products, conduct necessary studies and compile submission dossiers, including CMC part, (under the supervision of superiors, in case of Associate Scientist). In addition, expanding
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 Nippon Boehringer Ingelheim
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 Nippon Boehringer Ingelheim
Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the
Duties & Responsibilities ベーリンガーインゲルハイムの重点疾患領域であるメンタルヘルス領域では，まもなく上市する予定の薬剤を含めた複数のパイプラインを有しております。そのため，開発段階から上市後まで幅広くメディカル活動をリードするMA（Medical Advisor）を必要としています。グローバル戦略に沿い，複数の部署を横断するチームメンバーと協働しながら，エビデンス構築，専門家からのインサイトに基づくアンメットメディカルニーズの特定，アドバイザリーボード会議等の企画立案を責任者として担う役割です。この中で、日本の意見はグローバルの戦略に組み込まれますので、非常にやりがいのある仕事です。また、ドイツ本社メンバーとの国際会議や海外学会への参加など、海外のステークホルダーとのコミュニケーションも役割の一つです。 国内におけるメンタルヘルス領域のアンメットメディカルニーズを理解し，臨床研究の基本的な知識とプロジェクトを適切にマネージする能力，また他部署とのコラボレーションや外部専門家（External Experts）とのコミュニケーション，アドバイザリーボード会議や承認後の薬剤の価値最大化・適正使用に必要なメディカル戦略も検討していく長期的な視野を持った人材を求めています。 Jop profile for Medical Advisor: In Mental Helath Therapeutic Area of Boehringer ingelheim, we have multiple pipelines including a product will be launched shortly for this field. A Medical
Basic purpose of the job Insight Generation Manager is responsible for supporting therapeutic area teams with medical insight management. The role involves ensuring proper recording of scientific insights, resolving technical issues with insight capturing platforms, and
