CRA II
ICON plc
- Trabajo remoto
Senior CRA (Unblinded)
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 of treatments that benefit patients worldwide.
As a Clinical Research Associate (CRA) at ICON Plc , you will support and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards, with a focus on Unblinded studies .
What You Will Do:
You will perform clinical trial monitoring activities requiring technical expertise, with a focus on quality, compliance, and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing support and guidance to site staff to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
You will have a solid foundation in clinical trial monitoring, with specific experience working on Unblinded studies .
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- At least 1 year of experience as a Clinical Research Associate working on Unblinded studies .
- Strong understanding of clinical trial processes, monitoring practices, and regulatory requirements.
- Proven ability to manage multiple sites and activities simultaneously, with strong organizational and problem-solving skills.
- Excellent communication, interpersonal, and stakeholder management skills.
- Oncology experience is highly desirable.
- Willingness to travel as required (approximately 35%), including occasional travel within LATAM .
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
- Job Description Global Banking Client and Deal Support – Credit Product Delivery (CPD) – Transaction Execution Associate. Credit Product Delivery (CPD) is a middle office transaction management function within Global Banking, dedicated to supporting lending and...
- ...standards of care, competitive landscape, and local guidelines in the region. Evidence generation : Lead local evidence plans including IIS/IST support, RWE/HEOR projects, non‑interventional studies, and post‑authorization commitments in accordance with regulations and...
- ...The role is accountable for performance and compliance for assigned protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality...
- ...collaborating with business and technical stakeholders. Preferred Qualifications Salesforce certifications such as Platform Developer I/II, Sales Cloud Consultant, or Salesforce Administrator. Experience with enterprise-scale Salesforce implementations across multiple...
- ...study projects Strong experience leading and managing local, regional, and international vendors Previous experience as a Senior CRA Advanced English proficiency What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve...Trabajo remoto
- ...IQVIA is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Argentina Clinical Monitoring team. You will independently manage and monitor clinical trial sites to ensure studies comply with protocols, GCP, ICH guidelines, and regulatory requirements...
- ...IQVIA Biotech is hiring a Clinical Research Associate (CRA 2) for on-site monitoring in Argentina, focusing on oncology, cardiovascular, or internal medicine trials. You will monitor sites, ensure compliance with GCP/ICH, and support data integrity. Bachelor’s degree...
- ## 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...
- ...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 in Argentina. In this role, you will independently manage and monitor clinical trial sites to...
- ...Embark on your journey as a Trade Lifecycle Manager II where you'll be instrumental in managing the pre- and post-trading life cycle across all asset classes. Your expertise will ensure seamless trade processing and effective cash coordination, while your strong analytical...
- ...y zonas adyacentes de influencia, así como mitigar riesgos de corrupción de autoridades y funcionarios penitenciarios; Componente II: incrementar la cooperación transfronteriza de agencias de aplicación de la ley y justicia penal para potenciar investigaciones conjuntas...
- ...Syneos Health in Argentina is seeking a CTM II to oversee site management, clinical monitoring and central monitoring deliverables, with focus on patient safety, GCP compliance and data integrity. You will interact with CRAs, central monitors and investigators to ensure...
- Buenos Aires, Argentina Full time R1562678 Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical...
- ...Testing Site - JPMC is seeking an Application Support II within Intelligent Solutions Product Line in CTO. You will ensure operational stability, availability, and performance of production application flows, troubleshooting and resolving production service interruptions...
- ...coordination, and ongoing compliance amid frequent regulatory updates impacting trade and FX products. As a Trade Lifecycle Manager II within JPMorganChase, you will play a pivotal role in managing day-to-day operations supporting Foreign Trade (Comercio Exterior)...
- ...within your role and advance your career — and we have the perfect software engineering opportunity for you. As a Software Engineer II at JPMorganChase within the [insert LOB or sub LOB], you are part of an agile team that works to enhance, design, and deliver the...
- ...the management of a portfolio of Global Corporate Banking (”GCB”) and Investment Bank (“IB”) clients that have Asset Based loans and ii.) support in the independent analysis and review of credit exposure for new and existing ABL clients, in a second chair capacity until...
- ...tech backbone of our operations, where your expertise fuels seamless system functionality and innovation. As an Application Support II team member in Intelligent Solutions Product Line in CTO, you will play a vital role in ensuring the operational stability,...
- ...technologies Exposure to cloud technologies Your Role Level JPMorgan Chase is looking to hire Software Engineers at Software Engineer II and Software Engineer III levels. A determination will be made on placement for successful candidates based on the results of a...
- ...investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution.... ..., coaching and process execution. Description CTM II - ARG & CHL FSP Syneos Health® is a leading fully-integrated life...
- ...ask questions and execute compliance tasks in plain language. Trusted by companies operating across dozens of countries and SOC 2 Type II certified, they're positioning themselves as the operating infrastructure for any company running a global entity structure. About...
- ...JPMorganChase in Argentina is seeking a Software Engineer II to join an agile team and contribute to designing, developing, testing, securing, and delivering scalable software components for our state-of-the-art financial technology products, aligned with industry best...
- ...Business Development Representative to our Sales Development team in Buenos Aires ! The Business Development Representative II drives pipeline growth and new business generation within an assigned prospecting territory with a high level of autonomy. This role...
- ...innovation, operational needs, capacity, risk, and delivery feasibility when informing portfolio recommendations and trade-offs. II. Intake & Demand Management • Manage the end-to-end intake and demand process for analytics, automation, AI, technology, and...
- ...Evaluación de corrosión. -Integridad mecánica de activos. Validador de informes certificado API 570. Especialista END Nivel II o III Para respaldar los servicios de: -UT. -PA. -MT. -PT. -RT. -RT Digital. Responsable Higiene y Seguridad...
- ...CRA - All veleves | Vaccine 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...Trabajo remoto
- ...and Controls Schedule Full-time Employment Type : Employee Job Posting Oct 13, 2026 Reporting Manager Title: Manager II, Instrumentation Engineer Building on our past. Ready for the future Worley is a global company of energy, chemicals and...
- ...Medicine, Pharmacy, Biotechnology, QFB (Chemical Pharmaceutical Biology) or related health sciences ~1- 2 years of proven experience as a CRA monitoring clinical trials ~ Intermediate to advanced English proficiency (written and spoken) ~ Solid working knowledge of ICH-...
- Novo Nordisk A/S in Argentina seeks a Clinical Research Associate to support execution of clinical trials across the country. You will connect Novo Nordisk with trial sites, ensure studies meet global standards and patient safety remains the top priority. Responsibilities...
- ...Clinical Data Associate II role focused on managing and ensuring the quality of clinical trial data through review, reconciliation, and testing activities. The position supports day-to-day data management across multiple studies while collaborating with global teams,...
¿Desea recibir más vacantes?
Suscríbase y reciba vacantes similares a CRA II. ¡Sea el primero en aplicar!

