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
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
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
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
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Company Description PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time
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
Application Instructions: Please submit your resume in English when applying. Work Location Assignment: Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model. Colleagues are expected to work from the assigned Pfizer
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 d.o.o. is seeking a Records Management Compliance professional to manage TMF processes in a global context. You will handle document processing, reviews, and quality control to ensure regulatory compliance and high data integrity across
Worldwide Clinical Trials is seeking an Associate I, TMF Operations to support TMF processing, review and archiving of essential documents. The role involves working with electronic TMF systems and SharePoint to classify and maintain records across studies. The role requires
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 Limited is a global CRO seeking a Records Management Compliance Lead within the TMF Operations team. This role focuses on overseeing TMF quality, regulatory alignment, and collaboration with project teams and sponsors to ensure compliance
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.
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:
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:
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
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
Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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
When our values align, theres no limit to what we can achieve. Parexel FSP is looking for multiple Country Study Operations Manager I ! Candidates can be based anywhere in Mexico and Argentina. Job Summary The