某医薬品メーカーの薬剤投与に際し生じた副作用情報を専用システムに入力していくお仕事です。専門的な用語も生じますが未経験OK、貴重な経験と割り切れる方であれば全く問題ありません · ...

在宅勤務の一般事務・医薬品開発業務受託機関のお仕事です。週1回出社、未経験OKで安心のスタートができる環境です。 · ...

We are seeking a RegulatoryAffairs Specialist to join our team at JohnsonandJohnson.The successful candidate will be responsible for maintainingand managing regulatory approvals for pharmaceutical products including surgical suturesand adhesives. · ...

Leveraging the latest insights in pharmacokinetics (PK) and pharmacodynamics (PD), we apply advanced kinetic analysis to drive efficient drug development, regulatory registration and maximize compound value. · ...

+ · The company seeks an experienced professional for its regulatory affairs team responsible for maintaining management of Japan general surgery field products including sutures tissue adhesives etc. ...

+This role involves maintaining regulatory approvals for general surgery products including sutures and tissue adhesives. · +Promptly managing regulatory compliance activities across various regions. · Establishing strong relationships with key stakeholders within local authoriti ...

We are seeking an experienced PK specialist to join our team in Japan. As a PK specialist, you will play a critical role in driving efficient drug development and regulatory registration. · ...

A leading medical device/pharmaceutical company in the US with a rich welfare system seeks a Medical Affairs Manager based in Tokyo. · Building Clinical evidence · Identify clinical trial needs based on clinical strategy · Negotiate with KOL and cooperate with internal and exte ...

Leveraging advanced kinetic analysis to drive efficient drug development · and maximize compound value. · ...

Medical Affairs Manager at a medical device and pharmaceutical company in Tokyo, Japan. The company provides a range of products including medical devices, pharmaceuticals, and consumer goods. The role involves building clinical evidence, identifying clinical trial needs, and pla ...

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 Takadas Privacy Notice and Terms of Use. · ...

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? · ...

The CMC RA Manager will lead and manage CMC regulatory activities, develop and implement CMC registration strategies, and support the development of the CMCRA team. The ideal candidate will have +10 years of practical experience with CMC-related roles, experience drafting and com ...

Lead and manage CMC regulatory activities including relevant cross-functional communication, providing guidance across the product lifecycle, and ensuring timely regulatory compliance with official guidelines. Develop and implement CMC registration strategies related to CTNs, NDA ...

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. · Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is drive ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. · Lead the construction, ...

This position is responsible for conducting scientific evaluations of drug characteristics from a non-clinical perspective, developing domestic development strategies, and preparing materials to meet regulatory requirements. It also contributes to the implementation and approval ...

+Job summary · Nxera Group is an international biopharmaceutical company group focusing on drug discovery and initial development. · +ResponsibilitiesLead end-to-end evaluation of potential assets. · ...

An exciting opportunity to join Medtronic's Diabetes business unit as an Administrative Assistant I (DIAB @ Tokyo). This role involves supporting various administrative tasks related to product quality assurance. · ...

Nonclinica Project Specialist job description and requirements in Japan. · ...

Assistant Manager-Director/PVM/Japan to be responsible for product pricing and mathematical analysis, providing support to other departments and utilizing numerical skills. · ...