Senior Regulatory Submissions Translation PM
hace 2 semanas
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 Regulatory Submissions, and possess advanced client management skills. This role offers the opportunity to contribute to innovative healthcare solutions while working in a diverse and inclusive environment.#J-18808-Ljbffr
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Senior Translation PM: Regulatory Submissions
hace 2 semanas
Madrid, España IQVIA A tiempo completoA leading global provider of clinical research services is seeking a Senior Translation Project Manager to oversee the Regulatory Submissions translation and localization projects. Responsibilities include managing project lifecycles, working closely with clients, and ensuring high-quality standards. Ideal candidates will have a minimum of 4 years in Project...
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Senior Regulatory Submissions Translation Lead
hace 1 semana
Madrid, España IQVIA A tiempo completoA 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...
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Senior Translation Project Manager
hace 1 semana
Madrid, España IQVIA A tiempo completoSenior 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...
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Senior Translation Project Manager
hace 2 semanas
Madrid, España IQVIA LLC A tiempo completoSenior Translation Project Manager - Regulatory Submissions page is loaded## Senior Translation Project Manager - Regulatory Submissionslocations: Madrid, Spain: Barcelona, Spain: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R **SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS** Working with...
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Senior Translation Project Manager
hace 2 semanas
Madrid, España IQVIA A tiempo completoSENIOR 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 translation and localization projects to completion whilst ensuring...
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Senior Translation Project Manager
hace 2 semanas
Madrid, Madrid, España IQVIA A tiempo completoSENIOR 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 translation and localization projects to completion whilst ensuring...
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Senior Associate, Regulatory Submissions
hace 1 semana
Madrid, España Labcorp A tiempo completoResponsible 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...
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Regulatory Submissions Coordinator
hace 7 días
Madrid, España Medpace, Inc. A tiempo completoJob 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...
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Global Regulatory Submissions Specialist
hace 2 semanas
Madrid, España OPIS A tiempo completoAn International CRO is seeking a Regulatory Submissions Specialist to work remotely from Spain. The role involves managing regulatory submissions, contract negotiations, and ensuring compliance with industry standards. Candidates should have a minimum of 2 years of experience in clinical research and demonstrate fluency in English. The company offers a...
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Remote Global Regulatory Submissions Specialist
hace 2 semanas
Madrid, España OPIS A tiempo completoA leading international CRO is searching for a Regulatory Submissions Specialist to join their regulatory team. This position is remote, allowing flexibility. The ideal candidate will be fluent in English and have strong planning, problem-solving, and organizational skills. The role involves managing regulatory requirements, ensuring compliance, and...