Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Worldwide Clinical Trials in Argentina is seeking a Site Management professional to oversee clinical study site activities in line with GCP and applicable local and international regulations. You will support CTMs and field CRAs and coordinate
Worldwide Clinical Trials is seeking a Senior Associate I to support TMF Operations across global studies while upholding stringent compliance standards. You will lead TMF activities, collaborate with project teams and sponsors, and contribute to quality controls and documentation.
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Job Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted. You will be responsible for:
The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager II oversees and coordinates study resources to ensure compliance with the
The Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Project Manager I must ensure compliance with the study budget, project scope and timelines and in accordance
Buenos Aires, Argentina Full time R _IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine:_ _IQVIA Biotech