Orientamos nuestra búsqueda a quienes acrediten experiência en el área Investigaciones clínicas para trabajar en nuestro Hospital Universitario sede Saavedra. Serán sus principale…
El Administrador del Estudio Clínico (CSA) apoya la coordinación y administración de las actividades del estudio desde el inicio hasta la ejecución y el cierre, dentro del Equipo d…
El Administrador del Estudio Clínico (CSA) apoya la coordinación y administración de las actividades del estudio desde el inicio hasta la ejecución y el cierre, dentro del Equipo d…
ontribute to groundbreaking artificial intelligence research! We're recruiting participants for an important study developing technology that safeguards digital authenticity in an …
Job Summary: We are currently seeking a full-time, office-based **Clinical Research Project Coordinator** to join our Clinical Trial Management team. This position will work on a…
Job Summary Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team! This position p…
goFLUENT is revolutionizing the global language learning market, helping companies design a comprehensive digital training strategy for their employees. We accelerate language lear…
The Laboratory Logistics Specialist conducts logistics processes, in collaboration with other Laboratory Logistics personnel, ensuring that projects are progressing and systems are…
We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and…
The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Spons…
We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and…
Job Summary Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our m…
The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Spons…
**Job Overview**: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Opera…
Job Summary Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our ma…
The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Spons…
**Description** **Researched and relatable, science-driven and social, you’re an extroverted expert.** If there’s one thing your preparation in earning your advanced degree has…
**Position Description**: Student Support Advisors (SSA) work to create an inclusive environment that champions academic success and promotes Verto's core values of compassion, tr…
Join **Accenture** **and help transform leading organizations and communities around the world. Our **Corporate Functions** people offer the essential expertise to deliver high p…
**JOB DESCRIPTION**: - We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide …
Reciba por correo las últimas Ofertas de empleo en Buenos Aires