Regulatory Submissions

hace 4 semanas


Buenos Aires, Argentina Hitachi Vantara A tiempo completo

A global contract research organization is seeking a Country Approval Specialist to manage regulatory submissions and activate investigative sites. The candidate will provide advice on regulatory strategies and coordinate with internal teams to ensure timely site activation. A Bachelor’s degree and a minimum of 2 years of relevant experience are required. This role offers the chance to work in a dynamic environment focused on improving health outcomes worldwide.#J-18808-Ljbffr



  • Buenos Aires, Argentina Syneos Health A tiempo completo

    A leading biopharmaceutical company is seeking a Senior Regulatory Consultant to manage regulatory submissions and provide expert advice for clients in NA and LATAM. Responsibilities include regulatory writing, compliance assurance, and project management. This position offers a competitive salary range of $67,700 to $115,100 based on qualifications. The...


  • Buenos Aires, Argentina Syneos Health A tiempo completo

    A leading biopharmaceutical company is seeking a Senior Regulatory Consultant to manage regulatory submissions and provide expert advice for clients in NA and LATAM. Responsibilities include regulatory writing, compliance assurance, and project management. This position offers a competitive salary range of $67,700 to $115,100 based on qualifications. The...


  • Buenos Aires, Argentina Medpace A tiempo completo

    A leading clinical research organization in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join their Study Start Up team. This role involves managing all aspects of global start-up and requires at least 4 years of experience in regulatory submissions and strong leadership skills. You will collaborate with teams to contribute to...


  • Buenos Aires, Argentina Parexel A tiempo completo

    Regulatory Submissions Specialist (with Portuguese) IQVIA This role will require special working days as National Holidays and weekends. Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. You will review, assess, and process safety data and information received from various sources....


  • Buenos Aires, Argentina Medpace A tiempo completo

    A clinical research organization located in Buenos Aires is seeking a Regulatory Submissions Coordinator to support various clinical projects. The successful candidate will handle document collection, quality control, and ensure compliance with regulations. Applicants should have a Bachelor's degree in Life Sciences and 1-3 years of experience. The position...


  • Buenos Aires, Argentina BEON Tech Studio A tiempo completo

    Regulatory Submissions Specialist (with Portuguese) IQVIA This role will require special working days as National Holidays and weekends. Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources....


  • Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

    Department: Language ServicesSpecialization: Regulatory Submissions (Marketing Authorization)Location: Hybrid (Argentina, Latam and/or Canada)Employment Type: Full timeRole PurposeAs part of IQVIA's Project Management team, you will coordinate and manage the full lifecycle of Regulatory Submissions translation and localization projects for Marketing...

  • Regulatory Analyst

    hace 2 días


    Buenos Aires, Argentina The Gowan Co. A tiempo completo

    **Regulatory Analyst** **Position Summary**: The Regulatory Analyst supports the Regional Regulatory Manager in overseeing product registrations, ensuring compliance with regulatory standards, and facilitating the approval process for new and existing products. The role involves detailed analysis, coordination with internal teams, and the preparation of...


  • Buenos Aires, Argentina International Flavors & Fragrances A tiempo completo

    A clinical trial management firm in Buenos Aires is seeking a full-time Regulatory Submissions Manager to join the Study Start-Up team. This role requires at least 4 years of experience in regulatory submissions and strong communication skills. Responsibilities include managing global start-ups, quality checks on submission documents, and preparing informed...


  • Buenos Aires, Argentina Syneos Health, Inc. A tiempo completo

    A leading biopharmaceutical solutions organization is seeking a Senior Regulatory Consultant to support regulatory submissions and post-marketing activities. Located in Buenos Aires, Argentina, the ideal candidate must demonstrate regulatory writing and research skills. The position includes advising clients and managing projects, as well as involvement in...