clinical data associate

Parexel FSP is looking for CRAs to join our team in Argentina . We are looking for candidates with +1 year of monitoring experience, based in Buenos Aires. The Clinical Research Associate will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line...

Parexel FSP is looking for CRAs to join our team in Argentina . We are looking for candidates with +1 year of monitoring experience, based in Buenos Aires. The Clinical Research Associate will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line...

Parexel FSP is looking for CRAs to join our team in Argentina . We are looking for candidates with +1 year of monitoring experience, based in Buenos Aires. The Clinical Research Associate will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line...

ThermoFisher Scientific is seeking an entry-level Clinical Research Associate I to join our global team in Buenos Aires. You will perform and coordinate clinical monitoring activities, conduct on-site and remote visits, and manage essential trial documentation to ensure protocol adherence and data integrity. This role supports sites across sponsors and...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different...

We are seeking experienced Clinical Research Associates to join our team. As a CRA, you’ll be joining a fast-paced, driven environment that’s helping to make a life-changing difference to patients by ensuring high-quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the...

Fortrea is seeking a regulatory submissions specialist to act as the primary liaison with investigative sites. You will collect and quality-review essential documents for regulatory submissions and liaise with IRB/IEC and regulatory authorities under senior guidance. You will support in-country start-up activities, maintain study documents, and help adapt...

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials , we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around...

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the...

ThermoFisher Scientific is seeking an entry-level Clinical Research Associate I to join our global team in Buenos Aires. You will perform and coordinate clinical monitoring activities, conduct on-site and remote visits, and manage essential trial documentation to ensure protocol adherence and data integrity. This role supports sites across sponsors and...

ThermoFisher Scientific is seeking an entry-level Clinical Research Associate I to join our global team in Buenos Aires. You will perform and coordinate clinical monitoring activities, conduct on-site and remote visits, and manage essential trial documentation to ensure protocol adherence and data integrity. This role supports sites across sponsors and...