clinical data associate

Worldwide Clinical Trials is seeking a Clinical Trials Associate for a remote role available to candidates based in Argentina, Mexico, or Brazil. You will provide administrative and project-tracking support to clinical project teams, facilitating timely documentation, system access, and training coordination to keep studies inspection-ready.You will work...

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...

Fortrea is seeking a Site Monitor to oversee clinical studies in Argentina, ensuring adherence to SOPs, regulatory guidelines, and project plans. You will monitor sites, manage data integrity, and support site staff through monitoring visits.The role requires regulatory knowledge, English fluency, and the ability to work in a matrix environment, with travel...

Fortrea is seeking a regulatory submissions specialist to serve as primary contact with investigative sites, manage regulatory documents, and ensure timely submissions under ICH/GCP guidelines.The role involves coordinating with senior staff, vendors, and study teams to maintain compliance across country-specific requirements and prepare documents for...

IQVIA, un líder global en servicios de investigación clínica, insights y inteligencia sanitaria, busca colaborar en proyectos orientados a service delivery y mejoras de BI para clientes del sector life sciences.La posición implica análisis básico, desarrollo de cubos/tablas y conexión a dashboards en Power BI, con aprendizaje sobre metodologías de...

Thermo Fisher Scientific in Buenos Aires is seeking a Clinical Research Associate I (Entry Level) to support clinical monitoring and site management across trials. You will perform remote or on-site visits, ensure protocol compliance, and manage essential documents under ICH-GCP guidelines.This role offers exposure to diverse sponsors and monitoring...

Ofertas de Remote Clinical Research Associate ...Buenos Aires, ArgentinaFull timeR**Descripción General del Rol**Brinda un aporte oportuno y de alta calidad al desarrollo de soluciones para proyectos orientados a service delivery, managed services o implementación para clientes.Las asignaciones suelen requerir análisis básico y resolución de problemas,...

Grupo Jaka is seeking a Clinical Research Associate (CRA) to support site monitoring and study coordination for global projects. The role involves planning, initiation, monitoring and close-out visits with documentation, and regular communication with sites.Training and quarterly reviews are provided to guide performance, promotion, and bonuses. Requirements...

Syneos Health is seeking a Clinical Research Associate II to conduct on-site and remote monitoring of clinical studies, ensuring adherence to GCP and regulatory standards. You will develop monitoring tools, SOPs, and training materials while coordinating site visits and documentation.You will collaborate with investigators, site staff, and cross-functional...

¿Este trabajo es un acierto o un fracaso? Buenos Aires, Argentina Full time R **Descripción General del Rol** Brinda un aporte oportuno y de alta calidad al desarrollo de soluciones para proyectos orientados a service delivery, managed services o implementación para clientes. Las asignaciones suelen requerir análisis básico y resolución de problemas,...

Medpace is seeking a Clinical Research Associate in Buenos Aires to join our research-driven team. This role offers an exciting career in drug and medical device development, with travel across Argentina and entry into Medpace's CRA training program (PACE).No clinical experience may be required for the training pathway, with comprehensive initial and ongoing...

PSI in Argentina is seeking a Clinical Research Associate (CRA) to join our expanding team. You will have the opportunity to develop as a senior professional, trainer, mentor, and leader, with tailored courses and mentoring to advance your career.Responsibilities include monitoring visits, training site staff, working with complex studies, CRF review, and...

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...

Clinical Data Risk Analyst - Remote - Argentina At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development...

## Manager, Clinical Data ManagementApply: Remote: Buenos Aires, Argentina: Virtual Argentina: Full time: Posted Yesterday: JR103093**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 is built by...

Cordoba, ArgentinaFull timeR14664 About Us: Proofpoint is a global leader in human- and agent-centric cybersecurity. We protect how people, data, and AI agents connect across email, cloud, and collaboration tools. Over 80 of the Fortune 100, 10,000 large enterprises, and millions of smaller organizations trust Proofpoint to stop threats, prevent data loss,...

ICON is seeking a motivated FSP CRA I (Entry Level) in Buenos Aires to support remote and on-site trial activities. You will perform site monitoring, coordinate documentation, and ensure adherence to ICH-GCP guidelines across sponsors and study sites.Some travel to sites may be required. Ideal candidates hold a life sciences degree, demonstrate strong...

Fortrea seeks a Site Monitor to manage clinical study sites, ensuring protocol adherence, data integrity, and timely reporting. The role involves on-site monitoring, initiation/closeout visits, and liaising with vendors under SOPs and regulatory guidelines.The candidate should have a related degree and at least 6 months of experience, with proficiency in...

Parexel is seeking experienced Clinical Research Associates to join our team in a home-based role in Argentina. The CRA will monitor sites via on-site and remote visits, build strong investigator relationships, and collaborate with cross-functional teams to meet project timelines.The role requires a bachelor’s degree in life sciences and at least 1 year of...

Thermo Fisher Scientific is seeking an Assistant Clinical Research Associate in Buenos Aires to support site readiness, remote monitoring, and study coordination. You will assist with regulatory documents, training, and vendor coordination while ensuring adherence to SOPs and GCP guidelines.The role involves collaboration with CRA and Clinical Lead, some...