senior cra

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...

7257 Syneos Health Argentina S.A. is seeking a CRA SSU with at least 2 years of regulatory experience to support local submissions and regulatory activities in Argentina. The role requires working within the country team to ensure timely, compliant submissions and collaboration with project stakeholders.Join a global biopharmaceutical solutions leader with a...

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...

Precision Medicine Group in Argentina is expanding its Latin America capabilities and is seeking a Senior Clinical Research Associate to support critical studies across Argentina.The Senior CRA will bring broad experience in start-up, on-site monitoring, and ongoing site management, while mentoring junior staff and collaborating with Clinical Trial Managers....

Worldwide Clinical Trials is seeking a Clinical Research Associate II to operate on a home‑based basis supporting sites across Argentina. You will monitor across studies, ensure data integrity and regulatory compliance, mentor junior CRAs, and help drive study planning and training efforts.The role requires MD/Pharmacy or life sciences background with CRA...

IQVIA Biotech in Argentina is seeking a Senior Clinical Research Associate (Sr. CRA) with oncology preference to oversee site monitoring and study management.The role ensures conduct aligns with protocol, GCP, and sponsor requirements, including regular site visits and proactive communication. The candidate will monitor site performance, support regulatory...

PSI CRO is seeking a Clinical Research Associate I in Buenos Aires to conduct and report onsite monitoring visits, support feasibility studies, and manage site communications. You will perform CRF review and source data verification while coordinating with internal teams and vendor services.The ideal candidate has life sciences education, 1–2 years of...

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. ICON values integrity, collaboration, agility, and inclusion as core to its culture.As a CRA II/Senior CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data and...

IQVIA Biotech Argentina is seeking a dedicated Clinical Research Associate (CRA) to join our on-site team. The role focuses on monitoring clinical sites to ensure protocol compliance, regulatory alignment, and data integrity across oncology, cardiovascular, or internal medicine trials.Travel may be required and a minimum of 1 year on-site monitoring is...

IQVIA is seeking a Senior CRA to plan, execute, and manage clinical trials. The role focuses on data integrity, regulatory compliance, and trial success across multiple projects. You will monitor sites, support recruitment planning, and ensure protocol training.The position requires strong communication and the ability to work independently and with teams in...

Syneos Health Argentina S.A. is seeking a CRA II or Senior CRA (FSP) to perform site qualification, initiation, monitoring and close-out visits in Argentina from a home-based setting.You will evaluate site performance, ensure regulatory compliance, manage data quality, and support site staff with study activities. The role requires up to 75% travel, strong...

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IQVIA Biotech Argentina is hiring a Clinical Research Associate (CRA) 2 to monitor clinical sites on-site and ensure compliance with study protocols, GCP, and regulatory requirements. The role focuses on site visits, training, and data integrity across oncology, cardiovascular, or internal medicine trials.The ideal candidate has at least 1 year of on-site...

ICON Strategic Solutions in Argentina seeks an experienced Senior Clinical Research Associate to oversee monitoring activities and ensure trial conduct per protocol and GCP. You will travel ~30% to sites, manage multiple sites, and collaborate with cross-functional teams to support data quality and timeliness.You will be responsible for site visits, issue...

IQVIA Biotech is recruiting for a Senior Clinical Research Associate (Sr. CRA) in Argentina, oncology preferred. This role focuses on site monitoring and management to ensure study protocol compliance and data integrity across sites.The candidate will conduct monitoring visits, support subject recruitment plans, and maintain robust communication with study...

ICON is seeking a CRA II / Senior CRA to design and analyse clinical trials, interpreting complex medical data to advance therapies. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety across the trial lifecycle.You will collaborate with investigators and site...

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 CRA II / Senior CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.You will conduct...

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....

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...