Senior Regulatory Submissions Translation Lead

A global life sciences provider is seeking a Senior Translation Project Manager to coordinate Regulatory Submissions translation projects. You will manage multiple projects, liaise with clients, and ensure high quality standards. Ideal candidates have over 4 years of project management experience in the language services industry, expertise in regulatory...

A global leader in clinical research and healthcare intelligence is seeking a Senior Translation Project Manager for Regulatory Submissions in Madrid. You will manage multiple translation projects, ensuring high-quality standards and maintaining client relationships. Ideal candidates have over 4 years of experience in project management, particularly with...

Senior Translation Project Manager – Regulatory Submissions 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...

Senior Translation Project Manager – Regulatory Submissions 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...

Senior Translation Project Manager – Regulatory SubmissionsSENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONSWorking 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...

Responsible for providing support to regulatory managers and others for the timely submission of information to Regulatory Authorities in support of investigational and marketed products. Interacts with Regulatory Authorities and with clients to support regulatory activities. Proactively interacts with other Labcorp groups and with clients to provide...

A prominent pharmaceutical company in Madrid is seeking an experienced regulatory professional. The successful candidate will prepare and manage global regulatory submissions, ensuring compliance with EMA and ICH regulations. Familiarity with eCTD submissions and at least three years of prior experience in a regulatory role are essential. Strong...

Job Summary: 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 in Madrid. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise...

A leading biopharmaceutical solutions organization is seeking a Senior Regulatory Medical Writer to lead the completion of pivotal medical writing deliverables. This remote role requires excellent communication skills and a strong understanding of regulatory standards. Responsibilities include generating clinical study reports, protocols, and other essential...

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...