Empleos de cra en Buenos Aires

Your new roleAs a Clinical Research Associate, you'll play a critical role in the successful execution of clinical trials across Argentina. You'll be the vital link between Novo Nordisk and clinical trial sites, ensuring that our studies are conducted with integrity, in compliance with global standards, and with patient safety as the top priority.Your...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Select how often (in days) to receive an alert: Create AlertAs a Clinical Research Associate, you'll play a critical role in the successful execution of clinical trials across Argentina. You'll be the vital link between Novo Nordisk and clinical trial sites, ensuring that our studies are conducted with integrity, in compliance with global standards, and with...

CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a CRA II / Senior...

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.While Projects...

About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product...

CRA II - Sponsor dedicated - ArgentinaSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the...

CRA - Futures Roles (ARG) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, as one team, each the best...

IQVIA LLC is looking for a Clinical Research Associate (CRA) to advance your career with training and mentoring, enabling progression through performance reviews and bonuses. This role supports global projects with regional travel, offering a structured path and access to in-house technology.You will collaborate with colleagues and customers, with a focus on...

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team...

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 Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation! We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global...

Fortrea is seeking an experienced Clinical Monitoring professional to oversee site visits and data integrity for multiple studies. The role requires strong knowledge of ICH GCP, regulatory compliance, and hands-on CRA experience across monitoring activities.The position involves coordinating with study teams, preparing monitoring plans, and ensuring subject...

DescriptionCRA - Futures Roles (ARG)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Every day we perform better because of how we work together, as one team, each...

Novo Nordisk is seeking a Clinical Research Associate to oversee trials across Argentina, linking the company with trial sites to ensure integrity and patient safety. You will monitor sites, conduct initiation, routine visits, and close-outs while maintaining data quality for regulatory submissions.The role requires 1–2 years CRA experience, a health...

ICON Plc in Argentina is seeking a Senior Clinical Research Associate to oversee monitoring activities for sponsor-dedicated trials, ensuring adherence to protocol, regulatory requirements, and GCP standards.You will lead site visits, support cross-functional data collection and reporting, and train site staff to maintain high trial conduct, with travel up...

ICON Strategic Solutions is seeking a Clinical Research Associate I to contribute to our sponsor-dedicated clinical trial operations. You will deliver monitoring activities and help ensure high-quality data across programmes within ICON's global framework.You will coordinate site activities, manage sponsor queries, and support cost efficiency while...