Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. · Quality check on submission documents and site essential documents; · Interaction with US Cent ...

We are seeking a Principal Medical Writer to join our team in Clinical Development & Operations. · As a key member of our team, you will be responsible for authoring study-level clinical documents and individual clinical submission documents under the leadership of Senior Princip ...

Join our growing team as a Clinical Research Associate and receive training to become a fully functional CRA with the opportunity to work home-based. · Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; · ...

Toxicology Expert will assess preclinical toxicology data to ensure the safety of volunteers and patients participating in clinical trials in Japan, prepare high-quality toxicology documentation needed for initiating clinical trials, conducting PMDA consultations, and submitting ...

The Vice President, Regulatory Affairs Japan will contribute to the vision and goals of Global Regulatory Affairs (GRA) and ensure that Global Regulatory Affairs (GRA-J) Japan objectives are aligned with those. The role will provide leadership, strategic direction, and managerial ...

Join our growing team as a Clinical Research Associate and have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. · Clinical Research Associate - join our growing team · Are you a recent or upcom ...

This position provides environmental, health, and safety leadership to the Site. · ...

Deep Intelligent Pharma is pioneering the transformation of the pharmaceutical industry with a revolutionary AI-native, multi-agent platform. Our mission is to empower pharmaceutical and medtech innovators by turning regulatory and clinical complexity into a catalyst for speed, s ...

Join our growing team as a Clinical Research Associate (CRA) to conduct qualification initiation monitoring and closeout visits at research sites. · Conduct qualification initiation monitoring and closeout visits at research sites · Communication with medical site staff including ...

Executes a high-quality oversight of Pharmacovigilance (PV) governance by conducting below local process and compliance activities in alignment with global standards as well as Japanese regulation requirements · Audit/Inspection, CAPA management · QSD management · Training and Ar ...

Associate Director, GCP Compliance is responsible for directing and driving the implementation of regional compliance management related to quality events and internal audits for clinical trial delivery functions. · Direct and drive the implementation of regional compliance manag ...

Pharmacovigilance Officer responsible for conducting oversight of Pharmacovigilance governance, maintaining and implementing risk management activities, and supporting colleagues' activities. · Bachelor's degree or above · At least 3 years solid experience in pharmacovigilance ac ...

Direct and drive the implementation of regional compliance management related to quality events and internal audits for clinical trial delivery functions including the identification and development of applicable processes and tools. · Direct and drive the implementation of regio ...

This role is an exciting opportunity to join our fast-growing team as we further expand our footprint across Asia. Reporting to the Site Manager, Japan, this role will perform the fundamental function to keep operational readiness of DE's data center environment in daily operatio ...

Medpace is a leading CRO for biotech companies, adding leaders to its Clinical Trial Management team in Japan. Clinical Trial Managers with expertise in various therapeutic areas are welcome to continue working in their area of expertise or expand to a new one. · Effective manage ...

We are a skillful, driven and diverse team from across the globe, united by a passion to make an impact. Harnessing our innovative technologies and strong partnerships, we aim to make travel easy and rewarding for everyone. · Establish day to day communications with partner, conn ...

This position provides environmental, health, and safety leadership to the Site. Individual is accountable for directing EHS activities at his/her location(s); establishing EHS objectives and targets; internal reporting of EHS performance; communication of national, area, and loc ...

We're looking for an Operations Manager (Aviation Line Maintenance) to support our team. The Operations Manager will be responsible for overseeing all aspects of our line maintenance operations, ensuring the safe, efficient, and compliant execution of aircraft maintenance activit ...

This role puts you at the heart of our global growth strategy. You'll lead business development across regions, helping us bring smarter, safer thermal solutions to OEMs and Tier 1s. · Drive global business development initiatives aligned to our Automotive Strategy Plan · Prospec ...

Join a multicultural, bilingual setting, working on cutting-edge technologies that redefine the theme park experience. Work directly contributes to enhancing the overall guest experience. Create a holistic, technologically advanced environment where both external and internal cus ...

The Associate Director for Japan will develop and deploy Agoda's Japan strategy, provide guidance and leadership to ensure the successful account management of Agoda's major partners, and deliver on targets and growth expectations. · Develop and implement strategies to accelerate ...