Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level
Buenos Aires, Argentina São Paulo, Brazil Full time R We are seeking a highly motivated pharmacovigilance professional to join our Safety Aggregate Report & Analytics (SARA) team. This is an exciting opportunity to take a leading
Buenos Aires, Argentina São Paulo, Brazil Full time R Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial
Buenos Aires, Argentina Mexico City, Mexico São Paulo, Brazil Full time R Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and