Como Analista Sênior de Compliance em São Paulo, você liderará avaliações avançadas de riscos, implementará estratégias de conformidade e conduzirá investigações. Experiência prévia em serviços financeiros e conhecimento sólido em regulamentações são...
ClinChoice is seeking a Regulatory Affairs Associate Consultant. Coordinate regulatory projects, assist in preparing submissions, monitor updates, and ensure compliance efficiency. Bachelor's degree and 1 year of related experience required with stro...
Join dLocal as a Regulatory Compliance Officer in Brazil. Provide legal expertise on financial regulations, assess risks, and ensure regulatory compliance. Ideal for a professional with 5+ years of experience in the field. Join a global team driving ...
Senior Specialist in Regulatory Affairs and Study Start Up. Guide project teams on clinical study regulatory requirements, perform compliance assessments, adapt study documents, handle submissions to regulatory bodies, and ensure document quality. In...
The Sr. Study Start Up Associate leads local regulatory affairs activities, manages authority approvals, ensures compliance with local regulations, and provides guidance to study teams. Develops and submits required documentation, tracks progress, an...
The Technovigilance Specialist investigates customer complaints, classifies and reports them to comply with ANVISA regulations. Ensures completion of documentation, liaises with distributors, and monitors regulatory changes. Collaborates with Post Ma...
Manage regulatory strategies for new product launches in Brazil, lead submissions, stay updated on regulatory trends, review formulas and labels, and liaise with authorities. Requires a Bachelor's in a scientific field, prior cosmetics regulatory exp...
Join our dynamic team at PPD providing top-quality medical information services. As a Medical Information Specialist, you will offer technical support with superior customer service, adhering to regulatory guidelines. Expand your career in a collabor...
Join our exceptional team at PPD providing top-quality medical information services globally. Contribute to analyzing inquiries, handling adverse events, and ensuring compliance with regulatory standards. Benefit from career growth opportunities and ...
Join Veeva Systems as a Consultant in the Life Sciences sector, supporting software implementation projects globally. Utilize your consulting skills to drive efficiency and productivity for clients using R&D Suite for Clinical Operations, Regulatory,...
