Global Regulatory Submissions Specialist

A leading global CRO is seeking a Regulatory Submissions Specialist to join their team in a remote capacity. This role involves developing knowledge of regulatory requirements, managing contracts and budgets, and ensuring quality standards are met. Candidates should be fluent in English and possess strong planning, problem-solving, and organizational skills....

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he / she is involved in and ensures that the...

A global CRO is looking for a Regulatory Submissions Specialist to join their regulatory team remotely. The ideal candidate will manage regulatory submission activities, ensuring compliance with global and local requirements. The role demands fluency in English and strong planning and organizational skills. Experience in contract negotiation and procedural...

A pharmaceutical company in Madrid is seeking a Regulatory Affairs professional. The role involves managing regulatory submissions and ensuring compliance with pharmaceutical regulations. Key responsibilities include preparing and submitting regulatory dossiers, supporting product registrations, and collaborating with cross-functional teams. The ideal...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Graduate to join our Clinical Operations team as a Entry Level Regulatory Submissions Coordinator. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your...

A contract research organization is seeking a Senior Regulatory Affairs Specialist in Madrid to lead regulatory activities for clinical trials. This role involves overseeing complex global submissions, providing expertise to project teams, and mentoring junior colleagues. The ideal candidate has a Bachelor's degree, 3-5 years of regulatory experience, and a...

SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS Working with the wider Project Management team, the Senior Translation Project Manager – Regulatory Submissions is responsible for coordinating and managing the full lifecycle of Regulatory Submissions for Marketing Authorization translation and localization projects to completion whilst...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

Overview Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and / or part II following EU CTR and other applications created within or outside of the company to ensure documentation comply with applicable regulations and guidelines and...