Senior Regulatory Specialist

Job OverviewAs a Senior Regulatory Specialist, you will be responsible for ensuring that all regulatory requirements are met and that documentation is compliant with applicable regulations.The successful candidate will have primary contact with investigative sites during site start-up activities and maintenance. Your responsibilities will include the...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to develop and implement regulatory strategies for our products in Central and South America.Job DescriptionThe successful candidate will be responsible for managing regulatory submissions, maintaining compliance with local regulations, and collaborating with internal...

Job Title: Senior Regulatory Affairs Associate">In this role, you will be responsible for ensuring all labeling documents comply with regulatory standards and guidelines. This includes staying up-to-date on regulatory changes and industry best practices in labeling.">To succeed in this position, you will need to have the following qualifications and...

Regulatory Affairs SpecialistAre you passionate about ensuring the quality and compliance of medical products? Do you have experience in regulatory affairs and a strong understanding of ANVISA guidelines?We are seeking a highly organized and detail-oriented Regulatory Affairs Specialist to join our team. In this role, you will be responsible for assembling...

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulations and requirements. Develop stakeholder tools,...

Job Overview:The role of Senior Regulatory Specialist is pivotal in ensuring seamless site start-up activities and maintenance. This expert serves as the primary contact for investigative sites, guaranteeing timely collection of required documents and adherence to regulatory requirements.Key Responsibilities:Maintain awareness of current regulatory standards...

Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the timelines agreed with project management and Site...

Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the timelines agreed with project management and Site...

Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the timelines agreed with project management and Site...

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the timelines agreed with project management and Site...