CV Submission: Candidates must submit your CV in English . CVs in any other language will not be considered .

What You Will Be Doing:

- Overseeing the coordination and execution of shipments, deliveries, and inventory management for clinical trial materials.
- Developing and implementing logistics strategies to improve efficiency and reduce costs.
- Collaborating with vendors, suppliers, and internal teams to address and resolve logistics challenges.
- Monitoring and analyzing logistics performance metrics to identify opportunities for process improvements.
- Ensuring compliance with regulatory requirements and maintaining accurate shipping and inventory records.

Your Profile:

- Bachelor's degree in Logistics, Supply Chain Management, or a related field or equivalent experience.
- Proven experience in logistics coordination, with a strong understanding of supply chain and inventory management principles.
- Excellent organizational and problem-solving skills, with the ability to manage multiple projects and priorities.
- Strong communication and interpersonal skills, with a track record of working effectively with cross-functional teams and external partners.
- Proficiency in logistics software, data analysis tools, and Microsoft Office Suite.
- Advanced level of English

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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
- Versátil country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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.

FSP CRA I (Entry Level) - open for Study Coordinators, aCRA and CTAs

Buenos Aires ThermoFisher Scientific

Work Schedule
Standard (Mon-Fri)
Environmental Conditions




Office

Job Description
Join 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 team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You'll Do:

- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through phys

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