Senior Regulatory Submissions Translation PM

hace 2 días


Madrid, España IQVIA LLC A tiempo completo

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



  • Madrid, España IQVIA A tiempo completo

    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...


  • Madrid, España IQVIA A tiempo completo

    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...


  • Madrid, España IQVIA A tiempo completo

    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...


  • madrid, España IQVIA A tiempo completo

    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...


  • Madrid, España IQVIA A tiempo completo

    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...


  • Madrid, España Italfarmaco España A tiempo completo

    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...


  • Madrid, España Labcorp A tiempo completo

    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...


  • Madrid, España Medpace, Inc. A tiempo completo

    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...


  • Madrid, España Johnson & Johnson Innovative Medicine A tiempo completo

    A global healthcare leader is seeking an Experienced Regulatory Affairs Professional in Madrid. In this role, you will develop regulatory strategies and support submissions for innovative pharmaceutical products across EMEA. The ideal candidate has a Bachelor’s degree in Life Sciences or Pharmacy and 2+ years of relevant experience. Strong project...


  • Madrid, España Johnson & Johnson Innovative Medicine A tiempo completo

    A global healthcare leader is seeking an Experienced Regulatory Affairs Professional in Madrid. In this role, you will develop regulatory strategies and support submissions for innovative pharmaceutical products across EMEA. The ideal candidate has a Bachelor’s degree in Life Sciences or Pharmacy and 2+ years of relevant experience. Strong project...