A leading clinical research organization is looking for a full-time Clinical Safety Coordinator in Buenos Aires, Argentina. This position is critical to the pharmacovigilance process, requiring oversight of safety report submissions and in...
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 general start-up and requires at least 4 years of ...
A leading clinical research organization in Buenos Aires is seeking a full-time Site Contract Manager. This role involves managing contract teams, creating contract documents, and ensuring effective communication between stakeholders. Can...
A leading clinical research organization is looking for a full-time Clinical Safety Coordinator in Buenos Aires, Argentina. This position is critical to the pharmacovigilance process, requiring oversight of safety report submissions and int...
A leading clinical research organization in Buenos Aires is seeking a full-time Site Contract Manager. This role involves managing contract teams, creating contract documents, and ensuring effective communication between stakeholders. Candi...
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...
A clinical contract research organization is seeking a Regulatory Submissions Coordinator in Neuquen, Argentina. This role involves providing day-to-day support for regulatory submissions, ensuring compliance with applicable regulations, a...
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 ex...
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...