IHCRA Argentina (Hybrid mode)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
We are currently seeking an IHCRA to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

Location:

• Villa Adelina, Buenos Aires, Argentina (Hybrid mode: 3 days in the office and 2 days remote)

What you will be doing

• Assisting in the planning, initiation, and execution of clinical trial activities
• Conducting site feasibility assessments and participating in site selection processes
• Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
• Monitoring study progress and data collection activities to ensure quality and accuracy
• Assisting in the preparation and review of study documentation and reports

Your profile

• Bachelor’s degree in a relevant field, such as life sciences or healthcare
• Previous experience in clinical research or a related field preferred
• Strong organizational and communication skills
• Ability to work independently and collaboratively in a fast-paced environment
• Attention to detail and ability to prioritize tasks effectively

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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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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
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.

• Assisting in the planning, initiation, and execution of clinical trial activities
• Conducting site feasibility assessments and participating in site selection processes
• Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
• Monitoring study progress and data collection activities to ensure quality and accuracy
• Assisting in the preparation and review of study documentation and report