The Principal Scientist will manage teams with focus on policy and strategy implementation and control rather than development. · ...

We are partnering with a leading Chinese technology company to recruit talented researchers and scientists for their overseas R&D teams. · Responsibilities/h2>We are looking for a PhD holder with at least 3 years of work experience · ...

We are partnering with a leading Chinese technology company to recruit talented researchers and scientists for their overseas R&D teams.Selected candidates may have · the opportunity · to relocate to China in the future. · A PhD must have graduated before Jan 2023. · The candidat ...

Managing teams with focus on policy and strategy implementation and control rather than development. Short-term operational/tactical responsibilities. · ...

We are seeking an Associate Principal Scientist to lead clinical development projects in infectious diseases and vaccines. The successful candidate will have experience in clinical trial operations, clinical study design, learning sciences, negotiation, strategic thinking. · ...

+We are seeking an R&D Clinical Research Infectious Diseases Associate Principal Scientist with clinical development experience in related fields to lead clinical development projects for infectious diseases and vaccines. · This individual will collaborate closely with internal/e ...

This is a full-time role supporting drug discovery programs for global pharmaceutical partners.We are seeking talented scientists to join our Screening Unit. · ...

ALS × 新規遺伝子治療プラットフォームの創薬研究をリードする Founder 直属の上級サイエンティストを募集しています。 · 当社が支援する米国発バイオテックは、神経変性疾患の根本原因であるタンパク質ミスフォールディングに介入する革新的な遺伝子治療技術を開発しています。 · Founder の右腕として日本研究拠点の科学基盤を構築できる · ALS × 新世代遺伝子治療という "世界的ホット領域" の中枢で活躍 · コア科学に深く向き合える稀有な環境(企画ではなく、研究の本質に集中) · ...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. · I further attest that all information I su ...

We are hiring a Principal Technical Program Manager to help drive high-impact engineering projects with our customers and their partners, transforming their missions using AI and other cloud-based solutions and services.This work involves the development of broadly applicable, hi ...

We are seeking an experienced Data Scientist to join our Industry Solutions Engineering team in Tokyo. · The ideal candidate will have deep experience in developing and employing statistical and machine learning techniques to deliver business results.This role involves working wi ...

We are looking for a Principal Technical Program Manager to join our Industry Solutions Engineering team. · This role involves driving high-impact engineering projects with customers and their partners using AI and cloud-based solutions. · You will work closely with engineers fro ...

We are seeking a Clinical Scientist to join our team at Merck. As a medical responsible, you will provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study proto ...

Contribute to the TA strategy through researching the medical environment, identifying and building relationships with KEEs, and through the planning, preparation of advisory board meetings. Participate in program meetings to stay updated on the latest progress. · ...

MERCK is seeking a Medical Director to join their team. · Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study protocols and reports, Investigator Brochures ...

Lead, Local Trial Manager is a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience. This role is responsible for local management of a clinical trial (or Medical Affairs data generation ...

A Senior, Local Trial Manager is a mid-level trial management role with typically at least 2 years of clinical trial management or 3-5 years for clinical monitoring experience. This role is responsible for local management of a clinical trial (or Medical Affairs data generation a ...

Act as a medical responsible: Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study protocols and reports, Investigator Brochures, publications, etc. Act as ...

Do you enjoy meeting with customers to understand their needs and discuss the art of the possible? Then come join us to develop cloud-based solutions that can accelerate our customers' organizations. · ...

Act as a medical responsible: Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study protocols and reports, Investigator Brochures, publications, etc. Review ...

Join us as a Scientist/Senior Scientist, · Computational Chemistry in Cambridge, · MA, US or Fujisawa, · Kanagawa, · JAPAN. · ...