Empleos de cra en Buenos Aires

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...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...

Job DescriptionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.Performs clinical study site...

Job OverviewSite monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and...

## CRA 2, ArgentinaApplylocations: Buenos Aires, Argentinatime type: Full timeposted on: Posted Todayjob requisition id: R1540400***IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine:****IQVIA Biotech is a full-service CRO...

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 Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description CRA with at least 6 months in monitoring activities is preferred

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as an Assistant Clinical Research Associate – 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...

Job OverviewSite monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.ResponsibilitiesResponsible for all aspects of study site monitoring including routine monitoring and closeout of clinical...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionClinical Research professional with at least 1+ years of experience in the CRA role.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected...

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...

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...

Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionClinical Research professional with at least 1+ years of experience in the CRA role.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join 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...

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...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Research Associate (Level 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...

ICON Strategic Solutions in Buenos Aires is seeking a Clinical Research Associate I to join our sponsor-dedicated team. You will contribute to clinical trial monitoring across programmes, ensuring high-quality outcomes in a collaborative environment.You will manage site coordination, queries, and study documentation, while maintaining patient safety and...

IQVIA Biotech in Argentina is hiring a Senior Clinical Research Associate (Sr. CRA) with oncology experience to monitor trial sites and ensure compliance with protocol, regulations and sponsor requirements.The role involves site visits, recruitment tracking, training delivery, and collaboration with study teams. A Bachelor’s degree and 3–4 years on-site...

Merck is seeking an experienced Clinical Research Associate to act as the primary site contact and site manager across all trial phases. You will build strong site relationships, perform on-site monitoring, and ensure regulatory documentation aligns with ICH-GCP and Sponsor SOPs.You will collaborate with CRA teams and other sponsor functions to achieve Site...