Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical the ...

Seeking Regulatory Submissions Coordinator for full-time position in Tokyo. · ...

We are seeking a Regulatory Submissions Coordinator to join our Clinical Operations team in Japan. This position plays a key role in the clinical trial management process at Medpace. · Quality check on submission documents and site essential documents; · Interaction with US Centr ...

We are seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. · ...

The Manager, Regulatory Submissions manages high impact, complex submission projects involving multiple cross-functional regulatory submission teams. · Independently manages high impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ...

Senior Regulatory Legal Services Coordinator will provide professional company secretarial services to clients in Japan region with core areas of responsibility. The role will report to the Corporate Secretarial Manager. · Provide service to clients on company secretarial matters ...

The Regulatory Affairs Specialist will assess regulatory intelligence to assist in the development of local and global regulatory strategies. · BS in Engineering, Science or related degree; or MS in Regulatory Science · ...

Regulatory project role with regulatory affairs responsibilities in a pharmaceutical company. Develop regulatory strategy for new drug developments and provide regulatory expertise within project/product teams. · Develop regulatory strategy for new drug developments, · Health Aut ...

The Regulatory Affairs Manager is responsible for overseeing the preparation of regulatory submissions required to market new or modified devices in both domestic and international markets including all relevant maintenance activities.This position will also oversee the preparati ...

The team you will be joining plays an important role in the overall success of the organization. Across the globe, institutional investors rely on us to help them manage risk, respond to challenges, and drive performance and profitability. · Prior knowledge and experience of acco ...

· Provide scientifically rigorous statistical input into study design/plans/interpretation. · Develop effective collaborations within clinical teams/partner lines/external organizations. · ...

The Regulatory CMC Expert evaluates all CMC regulatory aspects related to the assigned products (including both development products and established products) in Japan. · The Regulatory CMC Expert develops and executes CMC strategies for development products/life-cycle management ...

Alber Blanc is an international prop high frequency trading company with more than 13 years of experience. We are seeking an experienced professional based in Japan to oversee local operations of a company focused on trading financial instruments on a part-time basis or full-time ...

We're proud to foster an inclusive environment driving innovation and excellence, · We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team.As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clin ...

The Cluster Senior Regulatory Affairs Manager will develop and maintain regulatory strategies for marketing authorization applications in cluster countries, ensuring compliance with global and regional requirements. The role involves monitoring operational progression of pre-mark ...

We're creating a healthier world for all people. For more than 35 years, · we've tackled diseases such as HIV, viral hepatitis, · Covid-19 and cancer – working relentlessly to develop · therapies that help improve lives and to ensure access · to these therapies across the globe.W ...

Join us if making your mark in the financial services industry from day one is a challenge you are up for. · We keep our clients at the heart of everything we do, · Own production and submission of the regulatory reporting to the local regulators including but not limited to FSA ...

We are looking for a passionate and detail-oriented Medical Writer to join our client in Japan. In this role, you will create high-quality scientific and regulatory documents that support drug development, clinical research, and medical communications. · Write, edit, and review c ...

+Job summary · Report to the Financial Controller Japan (Head of Finance), leading production and submission of regulatory reporting. · +Prior knowledge and experience of accounting and financial reporting. · Prior knowledge and solid understanding of regulatory reporting preferr ...

The R&D Regulatory Affairs has responsibility for managing products under development and/or marketed products with new indications. · ...

The Junior Compliance Officer plays a vital role in supporting the organization's compliance framework, focusing on regulatory reporting and filing, marketing material review, and employee compliance. · This position is suited for candidates with at least three years of experienc ...