Regulatory Affairs Specialist

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,...

Regulatory Affairs ExpertWe are seeking a highly skilled Regulatory Affairs Associate to join our team. This is an exciting opportunity for someone who is passionate about regulatory compliance and has excellent communication skills.Key Responsibilities:Demonstrate a thorough understanding of the structure and authorizing requirements for US Prescribing...

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...

As a Regulatory Affairs Associate at Parexel Consulting, you will support clinical trial submissions to regulatory authorities, focusing on projects in Brazil. This role offers an opportunity to develop skills in regulatory affairs and clinical research while working with experienced professionals.**Key Responsibilities**:- Contribute to high-quality...

**Regulatory Affairs Manager - LATAM**Elemental Enzymes (EE) is looking for a Regulatory Affairs Manager to develop regulatory strategy, manage regulatory submissions and maintain regulatory compliance for EE products in the Central and South American countries. Products include biopesticides, biostimulants, and biofertilizers. This position will report to...

Regulatory Affairs Associate Job SummaryWe are seeking a highly skilled and experienced Regulatory Affairs Associate to join our team. As a key member of our regulatory affairs team, you will be responsible for performing various tasks related to the submission of medicinal products to regulatory authorities.In this role, you will have the opportunity to...

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...

Job Overview:The primary contact with investigative sites during start-up activities and maintenance involves collecting required investigator and essential documents to ensure timely submission of EC/IRB/Third Body and Regulatory Authority applications. This role requires interaction with regulatory authorities to provide guidance on requirements and...

**Work mode**:Hybrid**Onsite Location(s)**:Brasília, DF, DF, BR**Additional Locations**: N/A**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**- At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the...

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...